ADJUSTABLE INTERSPINCRiS PROCESS BRACE

The present disclosure relates generally to orthopedics and orthopedic surgery More specifically, the present disclosure relates to devices used to support adjacent spinous processes

BACKGROUND

In human anatomy, the spine is a generally flexible column that can take tensile and compressive Scads The spine also allows bending motion and provides a place of attachment for keels, muscles and ligaments. Generally, the spine is divided into three sections' the cervical spine, the thoracic spine and the lumbar spine The sections of the spine are made up of individual bones called vertebrae. Also, the vertebrae are separated by intervertebral discs, which are situated between adjacent vertebrae.

The intervertebral discs function as shock absorbers and as joints. Further, the intervertebral discs can absorb the compressive and tensile loads to which the spinal column may be subjected. At the same time, the intervertebral discs can allow adjacent vertebral bodies to move relative to each other a limited amount, particularly during bendmg, or flexure, of the spine. Thus, the intervertebral discs are under constant muscular and/or gravitational pressure and generally, the intervertebral discs are the first parts of the lumbar spine to show signs of deterioration.

Facet joint degeneration is also common because the facet joints are in almost constant motion with the spine. In fact facet joint degeneration and disc degeneration frequently occur together. Generally, although one may be the primary problem while the other is a secondary problem resulting from the altered mechanics of the spine, by the time surgical options are considered, both facet joint degeneration and disc degeneration typically have occurred. For example, the altered mechanics of the facet joints and/or

intervertebral disc may cause spinal stenosis, degenerative spondylolisthesis, and degenerative scoliosis.

KI(J. 1 is a lateral view of a portion of a vertebral column;

FIG. 2 is a lateral view of a pair of adjacent vertrebrae;

FIG. 3 is a top plan view of a vertebra;

FIG. 4 is a plan view of a first adjustable interspinous process spacer in a retracted position,

FIG. 5 is a plan view of the firs! adjustable interspinous process spacer in an extended position;

FlG. 6 is a plan view of a second adjustable interspinous process spacer in a retracted position,

FlG. 7 is a plan view of the second adjustable interspinous process spacer in an extended position,

FKJ, 8 is a plan view of a third adjustable interspinous process spacer in a retracted position,

FIG. 9 is a plan view of the third adjustable interspinous process spacer in an extended position,

FIG. IO is a flow cbaii illustrating a first method of treating a spine;

FIG. 1 1 is a plan view of a fourth adjustable interspinous process spacer in a retracted position,

FIG. 12 is a plan view of the fourth adjustable interspinous process spacer in an extended position: and

FIG. 13 is a flow chart illustrating a second method of treating a spine.

DETAILED DESCRIPTION OF THE DRAWiNGS

An adjustable interspinous process brace is disclosed and can include a superior component. The superior component can include a superior spinous process bracket that can engage a superior spinous process. Portlier., the adjustable intervillous process brace can include an inferior component. The inferior component can include an inferior spinous process bracket that can engage an inferior spinous process, further, the inferior component can be movably engaged with the superior component from a retracted position to an extended position. In the extended position, a distance between the superior spinous process bracket and the inferior spinous process bracket can be increased.

In another embodiment, an adjustable interspinous process brace is disclosed and can include a superior spinous process bracket that can engage a superior spinous process. Also, the adjustable interspinous process brace can include an inferior spinous process bracket that can engage an inferior spinous process The inferior spinous process bracket can move relative to the superior spinous process bracket from a first position to a second position

In yet another embodiment, a method of treating a spine is disclosed and can include distracting a superior vertebra and an inferior vertebra Moreover, tlie method can include installing an adjustable interspinous process brace between a superior spinous process and an inferior spinous process and adjusting the adjustable interspinous process brace to support the superior spinous process and the inferior spinous process.

Sn still another embodiment, a method of treating a spine is disclosed and can include installing an adjustable interspinous process brace between a superior spinous process and an inferior spinous process Further, the method can include injecting an injectable biocompatible material into the adjustable interspinous process brace to increase a distance between the superior spinous process and the inferior spinous process.

In yet still another embodiment, an adjustable interspinous process brace is disclosed and can include a superior component. The superior component can include a

superior bracket thai can engage a portion of a superior vertebra Additionally, the adjustable mterspmous process brace can include an inferior component and the inferior component can include an inferior bracket that can engage a portion of an inferior \ertebra The inferior component can be rao\ably engaged with the superior component from a retracted position to an extended position in which a distance between the superior bracket and the inferior bracket can be increased

In another embodiment, a kit for field use is disclosed and includes an adjustable interspinous process brace that can have an interior chamber that can recehe an injectable biocompatible material The kit can also include an injectable biocompatible material

In still another embodiment, a kit for field use is disclosed and can include an adjustable interspinous process brace that can have an interior chamber that can recehe a spacer Further, the kit can include a plurality of spacers

Description of Relevant Anatomy

Referring initially to FlG 1, a portion of a vertebtal column, designated 100, is shown As depicted, the vertebral column !00 includes a lumbar region 102, a sacral region 104, and a coccygeal region 106 λs is known in the art, the vertebral column 100 also includes a corneal region and a thoracic region For claπty and ease of discussion, the cervical region and the thoracic region are not illustrated

λs shown in FfG I . the lumbar region 102 includes a first lumbar vertebra 108. a second lumbal \ ertebra 1 10, a third lumbar veπebra 1 12, a fourth lumbar vertebra 1 14, and a fifth lumbar vertebra 1 16 The sacral region 104 includes a sacrum 1 I S Further, the coccygeal region 106 includes a coccyx 120

As depicted in FlG 1, a first inten ertebral lumbar disc 122 is disposed between the fust lumbar vertebra 108 and the second lumbar \ertebia 110 A second intervertebral lumbar disc 124 is disposed between the second lumbar \ ertebra 1 10 and the third lumbar vertebra 1 12 A third intervertebral lumbar disc 126 is disposed between the third lumbar vertebra 1 12 and the fourth lumbar vertebra 1 14 Further a fourth intervertebral lumbar disc 128 is disposed between the fourth lumbar vertebra 1 14 and the fifth lumbar vertebra

1 16. Additionally, a fifth intervertebral lumbar disc 130 is disposed between the fifth lumbar vertebra 1 16 and the sacrum U 8.

In a particular embodiment, if one of the intervertebral lumbar discs 122, 124, 126, i28, 130 is diseased, degenerated, damaged, or otherwise in need of repair, treatment of thai intervertebral lumbar disc 122, 124, 126, 128, 130 can be effected in accordance with one or more of the embodiments described herein.

FIG. 2 depicts a detailed lateral view of two adjacent vertebrae, e g., two of the lumbar vertebra 108, 1 10, 1 12, 1 14, 1 16 shown in FlG 1. FlG 2 illustrates a superior vertebra 200 and an inferior vertebra 202. As shown, each vertebra 200, 202 includes a vertebral body 204, a superior articular process 206, a transverse process 20S, a spinous process 2 i0 and an inferior articular process 2 i 2. FIG. 2 further depicts an intervertebral disc 216 between the superior vertebra 200 and the interior vertebra 202

Referring to FlG, 3, a vertebra, e,g , the inferior vertebra 202 (FlG. 2), is illustrated. As shown, the vertebral body 204 of the inferior vertebra 202 includes a cortical rim 302 composed of cortical bone. Also, the vertebral body 204 includes cancellous bone 304 within the cortical rim 302. The cortical rim 302 is often referred Io as the apophyseal rim or apophyseal ring. Further, the cancellous bone 304 is softer than the cortical bone of the cortical rim 302.

As illustrated in FIG. 3, the inferior vertebra 202 further includes a first pedicle 306.. a second pedicle 308, a first iamina 310, and a second lamina 3 12. Further, a vertebral foramen 314 is established within the inferior vertebra 202. A spinal cord 316 passes through the vertebral foramen 314. Moreover, a first nerve root 318 and a second nerve root 320 extend from the spinal cord 3 ϊ6.

It is well known in the art that the vertebrae that make up the vertebral column have slightly different appearances as they range from the cervical region to the lumbar region of the vertebral column. However, all of the vertebrae, except the first and second cervical vertebrae, have the same basic structures, e.g , those structures described above in conjunction with FIG. 2 and FIG. 3. Hie first and second cervical vertebrae are structurally different than the rest of the vertebrae in order to support a skull.

Description of a First Embodiment of an Adjustable lnterspinous Process Brace

Referring to FlG, 4 and FlG. 5, a first adjustable interspinous process brace is shown and is generally designated 400. As shown, the adjustable interspinous process brace 400 includes an inferior component 402 and a superior component 404 In a particular embodiment, the components 402. 404 can be made from one or more biocompatible materials. For example, the materials can be metal containing materials, polymer materials, or composite materials that include metals, polymers, or combinations of metals and polymers.

In a particular embodiment, the metal containing materials can be metals. Further, the metal containing materials can be ceramics. Also, the metals can be pure metals or metal alloys. The pure metals can include titanium. Moreover, the metal alloys can include stainless steel, a cobalt-chrome-molybdenυm alloy, e.g., ASTM F-999 or ASTM F-75, a titanium alloy, or a combination thereof.

The polymer materials can include polyurethaπe materials, polyolefm materials, polyaryletherketone { PAEK) material s. silicone material s, hy drogel materials, or a combination thereof. Further, the poϊyoϊefin materials can include polypropylene, polyethylene, halogenated polyolefin, fiouropolyolefui. or a combination thereof The polyaryielherketon (PAEK) materials can include polyetherketone (PEK), poly ethereiher ketone (PEEK), polyetherketoneketone (PEKK), polyetherketoneetherketoneketone (PEKEKK), or a combination thereof The hydrogeis can include polyacryϊamide, poly-N-isopropylacrylamine, polyvinyl methyiether, polyvinyl alcohol, polyethyj hydroxy ethyl cellulose, poly (2-ethyl) oxazoline, polyetliyleneoxide, polyethylglyeol, polyethylene glycol, polyacrylic acid, polyaerylonitriie, polyvinyl acϊylate, polyvinylpyrrolidone, or a combination thereof. Alternatively, the components 402, 404 can be made from any other substantially rigid biocompatible materials.

As illustrated in FIG. 4 and FIG 5, the inferior component 402 can include an inferior support post 410. An inferior lateral arm 412 can extend from the inferior support

post 410 Further, an inferior spinous process bracket 414 can extend from the inferior 1 at era! arm 412

In a particular embodiment, the interior support post 410 can be hollow and can include an interior chamber 416 Moreover, a lateral cross-section of the inferior support post 410 can indicate that the inferi or support post 410 can be general Iy cy Sindrical

Alternative! j , the inferior support post 410 can have a cross-section that is generally prismatic Moreover the inferioi support post 410 can have any generally polyhedral shape w ith a central opening, or interior chamber, formed therein Also, the inferior support post 410 can include an injection port 418 established therein In a particular embodiment, the injection port 418 can lead to the interior chamber 4 i 6 and can he used to facilitate injection of a material into the interior chamber 416 within the inferior suppoit post 410

FICS 4 and FIG 5 show that the interior chamber 416 within the inferior support post 410 can include one or more corrugations 420 After a material is injected into the interior chamber 416 and cured, the corrugations 420 can substantially pievent relative motion between the cured material and the interior chamber 416

λs indicated in HG 4 and FICJ 5. the inferior spinous process bracket 414 can be generally U shaped Alterπaih eiy, the inferior spinous process bracket 414 can be generally V shaped Further, the inferior spinous process bracket 414 can include an inferior spinous process engagement structure 422 that extends from the inferior spinous process luacket 414 hi a particular embodiment, the inferior spinous process engagement structure 422 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process

Ph e inferior component 402 can also include a first inferior tether hole 430 and a second inferior tether hole 432 λn inferior tether 434 can span the inferior component

402. e g , between the first inferior tether hole 430 and the second inferior tether hole 432 Further, the inferior tether 434 can be looped at least partialis around a spinous process and can substantially maintain the spinous process in contact with the inferior spinous process bracket 414 In a particular embodiment, the inferior tether 434 can comprise a

biocompatible elastomeric material that flexes during installation and provides a resistance fit against the inferior process. Further, the inferior tether 434 can comprise a substantially non-resorbable suture or the like.

FIG. 4 and FIG. 5 a! so show that the inferior component 402 can include a hole 440 through the inferior support post 410 The hole 440 is configured to receive a locking pin, described below.

As illustrated in FlG. 4 and FIG. 5, the superior component 404 can include a superior support post 450, A superior lateral arm 452 can extend from the superior support post 450. Further, a superior spinous process bracket 454 can extend from the superior lateral arm 452.

In a particular embodiment, the superior support post 450 can be sized and shaped to fit into the inferior support post 4 iθ. Moreover, a lateral cross-section of the superior support post 450 can indicate that the superior support post 450 can be solid and generally cylindrical . Alternatively, the superior support post 450 can have a cross-section that is generally prismatic. Further, the superior support post 450 can have any generally polyhedral shape.

FlG. 4 and FlG. 5 indicate that the superior support post 450 can include a corrugated tip 456, After a material is injected into the interior chamber 416 within the inferior support post 410 and cured, the corrugated tip 456 can substantially prevent relative motion between the superior support post 450 and the cured material.

Accordingly, the corrugated tip 456 and the comigatϊons 420 formed within the interior chamber 416 can substantially prevent the superior support post 450 from being withdrawn, or otherwise pulled, from the interior chamber 416 within the inferior support post 410.

As indicated in FlG. 4 and FϊG, 5, the superior spinous process bracket 454 can be generally U shaped. Alternatively, the superior spinous process bracket 454 can be generally V shaped. Further, the superior spinous process bracket 454 can include a superior spinous process engagement structure 462 that extends from the superior spinous process bracket 454. In a particular embodiment, the superior spinous process

engagement structure 462 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process.

Hie superior component 404 can also include a first superior tether hole 470 and a second superior tether hole 472. A superior tether 474 can span the superior component 404, e.g., between the firs! superior tether hole 470 and the second superior tether hole

472. Further, the superior tether 474 can be looped at least partially around a spinous process and can substantially maintain the spinous process in contact with the superior spinous process bracket 454. In a particular embodiment, the superior tether 474 can comprise a biocompatible elastomeric material that flexes during installation and provides a resistance fit against the inferior process. Further, the superior tether 474 can comprise a substantially non-resorbable suture or the like. FIG. 4 and FlG 5 also show that the superior component 404 can include a plurality of holes 476 through the superior support post 450.

In a particular embodiment, one of the holes 476 in the superior support post 450 can be aligned with the hole 440 in the inferior support post 410 and a locking pin 478 can be inserted there through in order to substantially prevent any movement between the inferior component 402 and the superior component 404. Accordingly, the adjustable interspinous process brace 400 can be Socked in order to substantially resist compressive and tensile loads.

In a particular embodiment, when the adjustable interspinous process brace 400 is properly installed between a superior vertebra and an inferior vertebra, the inferior spinous process bracket 414 can engage and support an inferior spinous process 500. Further, the superior spinous process bracket 454 can engage and support a superior spinous process 502. More specifically, the inferior spinous process engagement structure 422 can extend slightly into and engage the inferior spinous process 500. Also, the superior spinous process engagement structure 462 can extend slightly into and engage the superior spinous process 502 Accordingly, the spinous process engagement structures 422, 462 and the tethers 434, 474 can substantially prevent the adjustable interspinous process brace 400 from migrating with respect to the spinous processes 500, 502

IO

Also, in a particular embodiment, the adjustable interspinous process brace 400 can be movable between a retracted position, shown in FIG. 4, and one or more extended positions, shown in FlG 5, In the retracted position, a distance 5 J 0 between the inferior spinous process bracket 414 and the superior spinous process bracket 454 can be at a minimum. However, when a material is injected into the interior chamber 416 within the inferior support post 410, the distance 510 between the inferior spinous process bracket 4 J 4 and the superior spinous process bracket 454 can be greater than when in the retracted position

Accordingly, the adjustable interspinous process brace 400 can be installed between an inferior spinous process 500 and a superior spinous process 502. Further, the superior component 404 can be moved relative to the inferior component 402, e.g., by injecting materia! into the interior chamber 416 within the inferior support post 410, in order to increase the distance between the superior spinous process 502 and the inferior spinous process 500.

Alternatively, a distractor can be used to increase the distance between the superior spinous process 502 and the inferior spinous process 500 and the adjustable interspinous process brace 400 can be adjusted to support the superior spinous process 502 and the inferior spinous process 500. After the adjustable interspinous process brace 400 is adjusted accordingly, the distractor can be removed and the adjustable interspinous process brace 400 can support the superior spinous process 502 and the inferior spinous process 500 to substantially prevent the distance between the superior spinous process 502 and the inferior spinous process 500 from returning to a pre-distraetion value. Further, the adjustable interspinous process brace 400 can dynamically resist compressive loads, tensile loads, or a combination thereof.

In a particular embodiment, the adjustable interspinous process brace 400 can be injected with one or more injectable biocompatible materials that remain elastic after curing. Further, the injectable biocompatible materials can include polymer materials that remain elastic after curing. Also, the injectable biocompatible materials can include ceramics.

For example, the polymer materials can include polyurefhane, polyolefin, silicone, silicone polyurethane copolymers, polymethylmethacrylate, epo.xy, cyanoacrylate, hydrogels, or a combination thereof. Further, the polyolefin materials can include polypropylene, polyethylene, halogenated poly olefin, and Oouropoiyolefin.

The hydrogels can include poly aery lamide (PAAM), poly-N~isopropyϊacryiamine

(PNlPAM), polyvinyl methylether (PVM), polyvinyl alcohol (PVA), polyethyl hydroxyelhyi cellulose, poly (2-ethyl) oxazoliπe, polyelliyleneoxide (PEO), polyethyiglycol (PEG), poiyacrylacid (PAA), polyacrylonitriie (PAN), poly vinylacry late (PVA), polyvinylpyrrolidone (PVP), or a combination thereof.

In a particular embodiment, the ceramics can include calcium phosphate, hydroxyapatite, calcium sulfate, bioactive glass, or a combination thereof. In an alternative embodiment, the injectable biocompatible materials cars include one or more fluids such as sterile water, saline, or sterile air.

In various embodiments, the injection port 418 can include a one-way valve (not shown) to allow passage of inj ectable material into the i nterior chamber 416 while substantially preventing expulsion or other movement of the injectable material from the interior chamber 416 through the injection port 418. Further, the injection port 416 can be configured to receive a plug, a screw, a bolt, a dowel, a combination thereof or another similar sealing device (not shown).

Description of a Second Embodiment of an Adjustable interspinous Process Brace

Referring to FϊG. 6 and FlG. 7, a second adjustable interspinous process brace is shown and is generally designated 600. As shown, the adjustable interspinous process brace 600 includes an inferior component 602 and a superior component 604. In a particular embodiment, the components 602, 604 can be made from one or more biocompatible materials. For example, the materials can be metal containing materials, polymer materials, or composite materials that include metals, polymers, or combinations of rn eta! s an d pol y m ers .

In a particular embodiment, the metal containing materials can be metals. Further, the metal containing materials can be ceramics. Also, the nietais can be pure metals or metal alloys. The pure metals can include titanium. Moreover, the metal alloys can include stainless steel a cobalt-chrome-molybdenum alloy, e.g., ASFM F -999 or ASTM F-75, a titanium alloy, or a combination thereof.

The polymer materials can include polyυrethane materials, polyoletln materials, polyaryielherketone (PAEK) materials, silicone materials, hydrogel materials, or a combination thereof. Further, the poly olefin materials can include polypropylene, polyethylene, halogenated polyolefin, flouropolyolefin, or a combination thereof. The polyaryletlierketon (PAKK ) materials can include polyetherketone ( PKK ). polyetheretherketone (PEEK), polyetherketoneketone (PEKK) ₅ polyetherketoneetherketoneketone (PEKEKK), or a combination thereof. The hydrogels can include polyacrylamide, poly-N-isopropylacryJamine, polyvinyl niethylether, polyvinyl alcohol, polyethyl hydroxyethyl cellulose, poly (2-ethyl) oxazoline, polyethyieneoxi de, poly etliylglycoh polyethyl ene glycol, polyacrylic aci d, polyaerySonitrile, polyvinyl aery late, polyvinylpyrrolidone, or a combination thereof. Alternatively, the components 602, 604 can be made from any other substantially rigid biocompatible material s.

As illustrated in FIG. 6 and FIG. 7, the inferior component 602 can include a first inferior support post 610 and a second inferior support post 612. A first inferior lateral arm 614 can extend from the first inferior support post 610 and a second inferior lateral arm 616 can extend from the second inferior support post 6 ! 2, Further, an inferior spinous process bracket 618 can extend between the first inferior lateral arm 614 and the second inferior lateral arm 616.

In a particular embodiment, the first inferior support post 610 can be hollow and can include a first interior chamber 620. A lateral cross-section of the first inferior support post 610 can indicate that the first inferior support post 650 can be generally cylindrical. Alternatively, the first inferior support post 610 can have a cross-section that is generally prismatic. Also, the first inferior support post 610 can have any generally polyhedral shape with a centra! opening, or interior chamber, formed therein. Also, the first inferior

support post 610 can include a first injection port 622 established therein. In a particular embodiment, the first injection port 622 can lead to the first interior chamber 620 and can be used to facilitate injection of a material into the first interior chamber 620 of the first inferior support post 610,

FIG. 6 and FIG. 7 show that the first interior chamber 620 within the first inferior support post 610 can include one or more corrugations 624. After a material is injected into the first interior chamber 620 and cured, the corrugations 624 can substantially prevent relative motion between the cured material and the first interior chamber 620.

In a particular embodiment, the second ulterior support post 612 can be hollow and can include a second interior chamber 630. A lateral cross-section of the second inferior support post 612 can indicate that the second inferior support post 612 can be generally cylindrical. Alternatively, the second inferior support post 612 can have a cross-section that is generally prismatic. Also, the second inferior support post 612 can have any generally polyhedral shape with a central opening, or interior chamber, formed therein. Also, the second inferior support post 612 can include a second injection port 632 established therein. In a particular embodiment, the second injection port 632 can lead to the second interior chamber 630 and can be used to facilitate injection of a material into the second interior chamber 630 within the second inferior support post 612.

FIG. 6 and FICJ. 7 show that the second interior chamber 630 within the second inferior support post 612 can include one or more corrugations 634. After a material is injected into the second interior chamber 630 and cured, the corrugations 634 can substantially prevent relative motion between the cured material and the second interior chamber 630,

As indicated in FlG. 6 and FIG. 7, the inferior spinous process bracket 618 can be generally U shaped. Alternatively, the inferior spinous process bracket 618 can be generally V shaped. Further, the inferior spinous process bracket 618 can include an inferior spinous process engagement staicture 640 that extends from the inferior spinous process bracket 618 In a particular embodiment, the i nferior spinous process engagement

structure 640 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process.

Hie inferior component 602 can also include an inferior tether 642 that can be wrapped around the inferior component 602, e.g., around the inferior spinous process bracket 618. In particular embodiment the inferior tether 642 can be looped at least partially around a spinous process and can substantially maintain the spinous process in contact with the inferior spinous process bracket 618. In a particular embodiment, the inferior tether 642 can comprise a biocompatible elastomer! c material that flexes during installation and provides a resistance fit against the inferior process Further, the inferior tether 642 can comprise a substantially non-resorbable suture or the like.

As illustrated in FlG. 6 and FIG. 7, the superior component 604 can include a first superior support post 650 and a second superior support post 652. A first superior lateral arm 654 can extend from the first superior support post 650 and a second superior lateral ami 656 can extend from the second superior support post 652. Further, a superior spinous process bracket 658 can extend between the first superior lateral arm 654 and the second superior lateral arm 656.

In a particular embodiment, the first superior support post 650 can be sized and shaped to fit into the first inferior support post 610 Moreover, a lateral cross- section of the first superior support post 650 can indicate that the first superior support post 650 can be solid and generally cylindrical. Alternatively, the first superior support post 650 can have a cross-section that is generally prismatic. Further, the first superior support post 650 can have any generally polyhedral shape.

FIG. 6 and FIG. 7 indicate that the first superior support post 650 can include a first corrugated tip 660, After a material is injected into the first interior chamber 620 within the first inferior support post 610 and cured, the first corrugated tip 660 can substantially prevent relative motion between the first superior support post 650 and the cured material Accordingly, the first corrugated tip 660 and the corrugations 624 formed within the first interior chamber 620 can substantially prevent the first superior support

post 650 from being withdrawn, or otherwise pulled, from the first interior chamber 624 within the first inferior support post 610.

In a particular embodiment, the second superior support post 652 can be sized and shaped to fit into the second inferior support post 612. Moreover, a lateral cross-section of the second superior support post 652 can indicate thai the second superior support post

652 can be solid and generally cylindrical Alternatively, the second superior support post 652 can have a cross-section that is generally prismatic. Further, the second superior support post 652 can have any generally polyhedral shape.

FIG. 6 and FIG. 7 indicate that the second superior support post 652 can include a second corrugated tip 670. After a material is injected into the second interior chamber

630 within the second inferior support post 612 and cured, the second corrugated tip 670 can substantially prevent relative motion between the second superior support post 652 and the cured material. Accordingly, the second corrugated tip 670 and the corrugations 634 formed within the second interior chamber 630 can substantially prevent the second superior support post 652 from being withdrawn, or otherwise pulled, from the second interior chamber 634 within the second inferior support post 612.

As indicated in FIG. 6 and FIG. 7, the superior spinous process bracket 658 can be generally U shaped. Alternatively, the superior spinous process bracket 658 can be generally V shaped. Further, the superior spinous process bracket 658 can include a superior spinous process engagement structure 680 that extends from the superior spinous process bracket 658. in a particular embodiment, the superior spinous process engagement structure 680 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process.

The superior component 604 can also include a superior tether 682 that can be wrapped around the superior component 604, e.g., around the superior spinous process bracket 658. In particular embodiment, the superior tether 682 can be looped at least partially around a spinous process and can substantially maintain the spinous process in contact with the superior spinous process bracket 658. In a particular embodiment, the superior tether 682 can comprise a biocompatible elastomeric material that flexes during

installation and provides a resistance fit against the superior process. Further, the superior tether 682 can comprise a substantially non-resorhabie suture or the like.

In a particular embodiment, when the adjustable interspinous process brace 600 is properly installed between a superior vertebra and an inferior vertebra, the inferior spinous process bracket 618 can engage and support an inferior spinous process 700. Further, the superior spinous process bracket 658 can engage and support a superior spinous process 702. More specifically, the inferior spinous process engagement structure 640 can extend slightly into and engage the inferior spinous process 700. Also, the superior spinous process engagement structure 680 can extend slightly into and engage the superior spinous process 702. Accordingly, the spinous process engagement structures 640, 680 and the tethers 642, 682 can substantially prevent the adjustable interspinous process brace 600 from migrating with respect to the spinous processes 700, 702.

Also, in a particular embodiment, the adjustable interspinous process brace 600 can be movable between a retracted position, shown in FIG. 6, and one or more extended positions, shown in FiG. 7. In the retracted position, a distance 710 between the inferior spinous process bracket 618 and the superior spinous process bracket 658 can be at a minimum. However, when a material is injected into the interior chambers 620, 630 within the inferior support posts 610, 612, the distance 710 between the inferior spinous process bracket 618 and the superior spinous process bracket 658 can be greater than when in the retracted position.

Accordingly, the adjustable interspinous process brace 600 can be installed between an inferior spinous process 700 and a superior spinous process 702. Further, the superior component 604 can be moved relative to the inferior component 602, e.g., by injecting material into the interior chambers 620, 630 within the inferior support posts 6K), 612, in order to increase the distance between the superior spinous process 702 and the inferior spinous process 700.

Alternatively, a distractor can be used to increase the distance between the superior spinous process 702 and the inferior spinous process 700 and the adjustable interspinous process brace 600 can be adjusted to support the superior spinous process 702 and the

inferior spinous process 700 After the adjustable interspinous process brace 600 is adjusted accordingly, the distractor can be rerøo\ed and the adjustable interspinous process brace 600 can support the superior spinous process 702 and the inferior spinous process 700 to substantial!} prevent the distance between the superior spinous process 702 and the inferior spinous process 700 from returning to a pre-distraction value Further, the adjustable interspinous process biace o00 can dynamically resist compressh e loads, tensile loads, or a combination thereof

In a particular embodiment, the adjustable interspinous process brace 600 can be injected with one or more injectable biocompatible materials that remain clastic after curing Further, the injectable biocompatible materials can include polymer materials that remain clastic after curing λlso, the injectable biocompatible materials can include ceramics

For example, the polymer materials can include polyurethane, polyolefm, silicone, silicone polyurethane copolymers, polymethylmethacrylate, epoxy, cyanoacrs late. In drogels, or a combination thereof Further, the polyolefin materials can include polypropylene, polyethylene, halogenated polyolefin, and fJouropolyolefirt

I he In drogels can include po!> aer\ lamide (PAλM), pol y-N4sopropyϊacry!amine (PNlPAMl po!>viny! metb> I ether (PVM), poly\ inyl alcohol (PYλl polyethyl hydsmyethyl cellulose, poly <2-eth>l) oxa/oline, polyethyleneoxide (PIiO). polyethylglvcol (PEG), poly aery 1 acid (PAA), polyacrylonitrile (PAN), polyvinj lacrylate

(PVA), polyvinylpyrrolidone (PVP), a\ a combination thereof

In a particular embodiment, the ceramtcs can include calcium phosphate, h\ droxy apatite, calcium sulfate, bioacthe glass, or a combination thereof In an alternative embodiment, the injectable biocompatible materials can include one or more fluids such as sterile water, saline, or sterile air

In various embodiments, each or both of the injection ports 622, 632 can include a onc-wa> valve (not shown) to allow passage of injectable material into the interior chambers 620. 630 while substantialh preventing expulsion or other movement of the injectable material from the interior chambers 620, 630 through the injection ports 622.

632. Further, the injection ports 622, 632 can be configured to receive a plug, a screw, a bolt, a dowel, a combination thereof or another simiiar sealing device (not shown).

Description of a Third Embodiment of an Adjustable ϊnterspinous Process Brace

Referring to RG. 8 and FICJ. 9, a third adjustable interspinoυs process brace is shown and is generally designated 800. As shown, the adjustable interspinous process brace 800 includes an inferior spinous process bracket 802 and a superior spinous process bracket 804. in a particular embodiment, the brackets 802, 804 can be made from one or more biocompatible materials For example, the materials can be metal containing materials, polymer materials, or composite materials that include metals, polymers, or combinations of metals and polymers.

In a particular embodiment, the metal containing materials can be metals. Further, the metal containing materials can be ceramics. Also, the metals can be pure metals or metal alloys. The pure metals can include titanium. Moreover, the metal alloys can include stainless steel, a cobalt-chrome-molybdenum alloy, e.g., ASTM F-999 or ASTM F-75, a titanium alloy, or a combination thereof.

The polymer materials can include polyurethane materials, polyolefin materials, polyaryletherketone (PAEK) materials, silicone materials, hydrogel materials, or a combination thereof. Further, the polyolefin materials can include polypropylene, polyethylene, halogenated polyolefin, fiouropolyolefm, or a combination thereof The polyarySetherketon (PAEK) materials can include polyether ketone (PEK), polyetheretherketone (PEEK), polyetherketoneketone (PEKK), polyetherketoneetherketoneketone (PKKEKK), or a combination thereof. The hydrogeis can include polyacrylamide, poly-N-isopropylacryiamine, polyvinyl methylether, polyvinyl alcohol, polyethy! hydroxyethy! cellulose, poly (2-ethyl) oxazoline, polyethyleneoxide, polyethy IgIy col, polyethylene glycol, polyacryiic acid, polyacrylonkrile, polyvinyl acrylate, polyvinylpyrrolidone, or a combination thereof. Alternatively, the brackets 802, 804 can be made from any other substantially rigid biocompatible materials.

As indicated in FlG. 8 and FlG. 9, the inferior spinous process bracket 802 can be generally V shaped and can include a first inferior support arm 810 and a second inferior support arm 812 Alternatively, the inferior spinous process bracket 802 can be generally U shaped. Further, the inferior spinous process bracket 802 can include an inferior spinous process engagement structure 814 that extends from the inferior spinous process bracket 802. In a particular embodiment, the inferior spinous process engagement structure 814 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process.

The inferior spinous process bracket 802 can also include a first inferior tether hole 820 and a second inferior tether hole 822. An inferior tether 824 can span the inferior spinous process bracket 802, e.g., between the first inferior tether hole 820 and the second inferior tether hole 822. Further, the inferior tether 824 can be looped at least partially around a spinous process and can substantially maintain the spinous process in contact with the inferior spinous process bracket 802. In a particular embodiment, the inferior tether 824 can comprise a biocompatible elastomeric material that flexes during installation and provides a resistance fit against the inferior process Further, the inferior tether 824 can comprise a substantially non-resorbable suture or the like.

Further, the superior spinous process bracket 804 can be generally V shaped and can include a first superior support arm 830 and a second superior support arm 832. Alternatively, the superior spinous process bracket 804 can be generally U shaped The superior spinous process bracket 804 can also include a superior spinous process engagement structure 834 that extends from the superior spinous process bracket 804. In a particular embodiment, the superior spinous process engagement structure 834 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process

The superior spinous process bracket 804 can also include a first superior tether hole 840 and a second superior tether hole 842 A superior tether 844 can span the superior spinous process bracket 804, e g., between the first superior tether hole 840 and the second superior tether hole 842. Further, the superior tether 844 can be looped at least partially around a spinous process and can substantially maintain the spinous process in

contact with the superior spinous process bracket 804. In a particular embodiment, the superior tether 844 can comprise a biocompatible eiastonieric material that flexes during installation and provides a resistance fit against the superior process Further, the superior tether 844 can comprise a substantially non-resorbable suture or the like

FIG. S and FIG 9 indicate that the adjustable interspinous process brace 800 can include a first inflatable member 850 disposed between the first inferior support ami 810 and the first superior support arm 830. The first inflatable member 850 can include an injection port 850 Further, the first inflatable member 850 can be inflated via the injection port 852.

Additionally, the adjustable interspinous process brace 800 can include a second inflatable member 860 disposed between the second inferior support arm 812 and the second superior support arm 832. The second inflatable member 860 can include an injection port 862. Further, the second inflatable member 860 can be inflated via the injection port 862.

In a particular embodiment, when the adjustable i nterspi nous process brace 800 i s properly installed between a superior vertebra and an inferior vertebra, the inferior spinous process bracket 802 can engage and support an inferior spinous process 900 Further, the superior spinous process bracket 804 can engage and support a superior spinous process 902. More specifically, the inferior spinous process engagement structure 814 can extend slightly into and engage the inferior spinous process 900, Also, the superior spinous process engagement structure 834 can extend slightly into and engage the superior spinous process 902. Accordingly, the spinous process engagement structures 814, 834 and the tethers 824, 844 can substantially prevent the adjustable interspinous process brace 800 from migrating with respect to the spinous processes 900, 902

Also, in a particular embodiment, the adjustable interspinous process brace 800 can be movable between a collapsed position, shown in FlG 8, and one or more inflated positions, shown in FlG 9. In the collapsed position, a distance 910 between the inferior spinous process bracket 802 and the superior spinous process bracket 804 can be at a minimum. However, when a material is injected into the inflatable members 850, 860, the

distance 910 between the inferior spinous process bracket 802 and the superior spinous process bracket 804 can be greater than when in the collapsed position.

Accordingly, the adjustable interspinous process brace 800 can be installed between an inferior spinous process 900 and a superior spinous process 902. Further, the superior spinous process bracket 804 can be moved relative to the inferior spinous process bracket 802, e.g., by injecting material into the inflatable members 850, 860, in order to increase the distance between the superior spinous process 902 and the inferior spinous process 900. In various embodiments, the inflatable members 850, 860 can be physically fastened or adhered (e.g., with an adhesive) to the spinous process brackets 802, 804, in order to prevent migration of the inflatable members while in use.

Alternatively, a distractor can be used to increase the distance between the superior spinous process 902 and the inferior spinous process 900 and the adjustable imerspinous process brace 800 can be adjusted to support the superior spinous process 902 and the inferior spinous process 900. After the adjustable interspinoυs process brace SOO is adjusted accordingly, the distractor can be removed and the adjustable inferspinous process brace 800 can support the superior spinous process 902 and the inferior spinous process 900 to substantially prevent the distance between the superior spinous process 902 and the inferior spinous process 900 from returning to a pre-distraction value. Further, the adjustable interspinoυs process brace 800 can dynamically resist compressive loads, tensile loads, or a combination thereof

In a particular embodiment, the adjustable interspinous process brace 800 can be injected with one or more injectable biocompatible materials that remain elastic after curing. Further, the injectable biocompatible materials can include polymer materials that remain elastic after curing. Also, the injectable biocompatible materials can include ceramics.

For example, the polymer materials can include polyυrethane, polyolefm, silicone, silicone polyurethane copolymers, polymethylmethacrylate, epoxy, cyanoacrylate, hydrogels, or a combination thereof. Further, the polyolefm materials can include polypropylene, polyethylene, halogenated polyolefm, and flouropolyoletin.

The hydrogels cars include polyacrylamide (PAAM), poly-N-isopropy!acrylamine (PNIPAM), polyvinyl methyl ether (PVM), polyvinyl alcohol (PVA), polyethyl hydroxyethyl cellulose, poly (2-ethylj oxazoline, polyethyleneoxide (PEO), polyeihylglycol (PEG), polyacrylacid (PAA), polyacrylomtriie (PAN), polyvinylacrylate (PVA), polyvinylpyrrolidone (PVP), or a combination thereof.

In a particular embodiment, the ceramics can include calcium phosphate, hydroxyapatite, calcium sulfate, bioactive glass, or a combination thereof. In an alternative embodiment, the injectable biocompatible materials can include one or more fluids such as sterile water, saline, or sterile air.

. In various embodiments, each or both injection ports 852, 862 can include a oneway valve (not shown) to allow passage of injectable material into the inflatable members 850, 860 while substantially preventing expulsion or other movement of the injectable material from the inflatable members 850, S60 through the injection ports 852, 862 Further, the injection ports 852, 862 can be configured to receive a plug, a screw, a bolt, a dowel, a combination thereof or another similar sealing device (not shown).

Description of a First Method of Treating a Spine

Referring to FlG. 10, a method of treating a spine is shown and commences at block 1000. At block 1000, a patient can be secured in a prone position, e.g., on an operating table. At block 1002. the posterior spine can be exposed in order to expose adjacent spinous processes. Further, at block 1004, a surgical retractor system can be installed to keep a surgical field open.

Moving to block 1006, a superior vertebra and inferior vertebra can be distracted. In a particular embodiment, the superior vertebra and inferior vertebra can be distracted using a distractor. At block 1008, a distance between the adjacent spinous processes can be measured. Thereafter, at block 1010 it is determined whether the distraction is correct, e g , has the superior vertebra and inferior vertebral been distracted such that a distance between the adjacent spinous processes has reached a value that a surgeon has deemed therapeutic. For example, the superior vertebra and inferior vertebra can be distracted in order to reduce or obviate impingement on a nerve root.

If the distraction is not correct, the method can return to block 1006 and the superior vertebra and inferior vertebra can be further distracted. Conversely, if the distraction is correct, the method can move to block J 012 and an adjustable interspinous process brace can be installed between the adjacent spinous processes.

Proceeding to block 1014, a material can be injected into the adjustable interspinous process brace. In a particular embodiment, the adjustable interspinous process brace can be injected with one or more injectable biocompatible materials that remain elastic after curing. Further, the injectable biocompatible materials can include polymer materials that remain elastic after curing Also, the injectable biocompatible materials can include ceramics.

For example, the polymer materials can include polyurethane, polyolefin, silicone, silicone polyurethane copolymers, polymethylmethacrylate, epoxy, cyanoacrylate, hydrogels, or a combination thereof. Further, the poiyoiefm materials can include polypropylene, polyethylene, halogenated poiyoiefm, and fiouropojyolefjn.

The hydrogels can include polyacryl amide (PAAM), poly-N-isopropylacrylarnine

(PNlPAM) ₅ polyvinyl rnethylether (PVM), polyvinyl alcohol (PVA), polyethyi hydroxyethyi cellulose, poly (2-ethyl) oxazoline, polyetliyleneoxide (PEO), polyethylglycol (PEG), poiyacrylacid (PAA), poly aery ioni true (PAN), poly vinylacry late (PVA), polyvinylpyrrolidone (PVP), or a combination thereof,

In a particular embodiment, the ceramics can include calcium phosphate, hydroxyapatite, calcium sulfate, bioactive glass, or a combination thereof. In an alternative embodiment, the injectable biocompatible materials can include one or more fluids such as sterϋe water, saline, or sterile air.

Moving to decision step 1016 it can be determined whether the adjustable interspinous process brace fits correctly into the space between the adjacent spinous processes. If not. the method can return to block 1014 and more material can be injected into the adjustable interspinous process brace. On the other hand, if the adjustable interspinous process brace fits correctly between the adjacent spinous processes, the method can proceed to block 1018.

At block 1018, one or more injection ports can be sealed. In a particular embodiment, simply curing the materia! within the adjustable interspinous process brace can seal the one or more injection ports. Alternatively, a plug, a screw, a bolt, a dowel, a combination thereof, or another similar device can be used to sea! the one or more injection ports. Further, a one-way valve can be incorporated into each injection port arid can allow material to be injected into the adjustable interspinous process brace, but prevent the same material from being expelled from the adjustable interspinous process brace.

Continuing to block 1020, the surgical area can be irrigated At block 1022, the retractor system can be removed. Further, at block 1024, the surgical wound can be closed. The surgical wound can be closed by simply allowing the patient ^' s skin to close due to the elasticity of the skin Alternatively, the surgical wound can be closed using sutures, surgical staples, or any other suitable surgical technique well known in the art At block 1026. postoperative care can be initiated. The method can end at state 1028

Description of a Fourth Embodiment of an Adjustable Interspinous Process Brace

Referring to FKJ 1 1 and FIG. 12 ₅ a fourth adjustable interspinous process brace is shown and is generally designated 1 100, As shown, the adjustable interspinous process brace 1 100 includes an inferior component 1102 and a superior component 1 104 In a particular embodiment, the components 1 102.. 1 104 can be made from one or more biocompatible materials. For example, the materials can be metal containing materials, polymer materials, or composite materials that include metals, polymers, or combinations of metals and polymers.

In a particular embodiment the metal containing materials can be metals Further, the metal containing materials can be ceramics. Also, the metals can be pure metals or metal alloys The pure metals can include titanium. Moreover, the metal alloys can include stainless steel, a cobalt-chrome-molybdenum alloy, e.g., ASTM F- ^Q 99 or ASTM F-75, a titanium alloy, or a combination thereof

The polymer materials can include polyurethane materials, polyolefln materials, polyaryletherketone (PAEK) materials, silicone materials, hydrogel materials, or a

combination thereof Further, the polyolefin materials eart include polypropylene, polyethylene, halogenated poiyoiefin, flouropolyolefm, or a combination thereof. The polyaryletherketon (PAEK) materials can include polyetherk clone (PEK), polyetheretherketone {PEEK), polyetherk etoneketone (PEKK). polyetherk etoneetherketoneketone (PEKEKK), or a combination thereof. The hydrogels can include poly aery iamide, poly-N-isopropylacrylarame, polyvinyl melhylether, polyvinyl alcohol, polyethyi hydroxyethyl cellulose, poly (2 -ethyl) oxazoline, polyethyleneoxide. polyethylglycoi, polyethylene glycol, poiyacrylic acid, polyaerylonitrile, polyvinylaerylate, polyvinylpyrrolidone, or a combination thereof. Alternatively, the components 1 102, 1 104 can be made from any other substantially rigid hi oeom pati bl e material s .

As illustrated in FIG. 1 1 and FlG. 12, the inferior component 1 102 can include a first inferior support post 1 1 10 and a second inferior support post 1 1 12. A first interior lateral arm 1 1 14 can extend from the first inferior support post 1 1 10 and a second inferior lateral arm 1 1 16 can extend from the second inferior support post 1 1 12. Further, an inferior spinous process bracket ! 1 18 can extend between the first inferior lateral arm 1 1 14 and the second inferior lateral arm 1 1 16.

In a particular embodiment, the first inferior support post 1 1 10 can be hollow and can include a first interior chamber 1 120. A lateral cross-section of the first inferior support post 1 1 10 can indicate that the first inferior support post U lO can be generally cylindrical Alternatively, the first inferior support post S 110 can have a cross-section that is generally prismatic. Also, the first inferior support post 1 1 10 can have any generally polyhedral shape with a central opening, or interior chamber, formed therein.

As shown in FlG. 1 1 and FlG. 12, one or more spacers 1122 can be disposed within the first interior chamber 1120 In a particular embodiment, the spacers 1 122 can be elastic. Further, the spacers 1 122 can be spherically shaped, cube shaped, disc shaped, or a combination thereof

In a particular embodiment, the second inferior support post 1 1 12 can be hollow and can include a second interior chamber 1 130, A lateral cross-section of the second

inferior support post 1 1 12 can indicate that the second inferior support post 1 1 12 can be hollow and generally cylindrical. Alternatively, the second interior support post U 12 can have a cross-section that is generally prismatic. Also, the second inferior support post 1 112 can have any generally polyhedral shape with a central opening, or interior chamber. formed therein.

As shown in FfG i 1 and FIG. 12, one or more spacers 1 132 can be disposed within the first interior chamber 1 130. In a particular embodiment, the spacers 1 132 can be elastic. Further, the spacers 1 132 can be spherically shaped, cube shaped, disc shaped, or a combination thereof

As indicated in FlG 1 1 and FlG. 12. the inferior spinous process bracket 1 1 18 can be generally U shaped Alternatively, the inferior spinous process bracket 1118 can be generally V shaped. Further, the inferior spinous process bracket 11 18 can include an inferior spinous process engagement structure 1 140 that extends from the inferior spinous process bracket 1 1 18. in a particular embodiment, the inferior spinous process engagement structure 1 140 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process.

The inferior component 1 102 can also include an inferior tether 1142 that can be wrapped around the inferior component 1 102, e.g., around the inferior spinous process bracket 1 1 18. In particular embodiment, the inferior tether 1 142 can be iooped at least partially around a spinous process and can substantially maintain the spinous process in contact with the inferior spinous process bracket 1 1 18. ϊn a particular embodiment, the inferior tether 1142 can comprise a biocompatible elastomeric material that flexes during installation and provides a resistance fit against the inferior process. Further, the inferior tether 1 142 can comprise a substantially non-resorbabie suture or the like,

As illustrated in FKJ 1 1 and FIG. 12, the superior component 1 104 can include a first superior support post 1 1 50 and a second superior support post i 152. A first superior lateral arm i 1 54 can extend from the first superior support post 1 150 and a second superior lateral arm 1 1 56 can extend from the second superior support post 1 152 Further,

a superior spinous process bracket 1 158 can extend between the first superior lateral arm 1 1 54 and the second superior lateral arm 1 156.

In a particular embodiment, the first superior support post 1 150 can be sized and shaped to fit into the first inferior support post 1 1 10. Moreover, a lateral cross-section of the first superior support post 1 150 can indicate that the first superior support post 1 150 can be solid and generally cylindrical Alternatively, the first superior support post 1 J 50 can have a cross-section that is generally prismatic. Further, the first superior support post 1 1 50 can have any generally polyhedral shape.

In a particular embodiment, the second superior support post 1 152 can be sized and shaped to fit into the second inferior support post 1 1 12. Moreover, a lateral cross-section of the second superior support post 1152 can indicate that the second superior support post 1 152 can be solid and generally cylindrical Alternatively, the second superior support post 1 152 can have a cross-section that is generally prismatic. Further, the second superior support post 1 152 can have any generally polyhedral shape.

As indicated in FlG. 1 1 and FlG. 12, the superior spinous process bracket 1 158 can be generally U shaped. Alternatively, the superior spinous process bracket 1 158 can be generally V shaped. Further, the superior spinous process bracket 1 158 can include a superior spinous process engagement structure 1 180 that extends from the superior spinous process bracket 1 158. In a particular embodiment, the superior spinous process engagement structure 1 180 can be one or more spikes, one or more teeth, a combination thereof, or some other structure configured to engage a spinous process.

The superior component 1 104 can also include a superior tether 1 182 that can be wrapped around the superior component 1 104, e.g., around the superior spinous process bracket 1 158, ϊπ particular embodiment, the superior tether 1 182 can be looped at least partially around a spinous process and can substantially maintain the spinous process in contact with the superior spinous process bracket 1 158 In a particular embodiment, the superior tether 1 182 can comprise a biocompatible elastomeric material that flexes during installation and provides a resistance fit against the superior process. Further, the superior tether 1 182 can comprise a substantially non~resorbab!e suture or the like.

In a particular embodiment, when the adjustable interspinous process brace 1 100 is properly installed between a superior \ertebra and an inferior vertebra, the inferior spinous process bracket 1 118 can engage and support an inferior spinous process 1200 Further, the superior spinous process bracket 1 158 can engage and support a superior spinous process 1202, More specifically, the inferior spinous process engagement structure 1 140 can extend slightly into and engage the inferior spinous process 1200. Also, the superior spinous process engagement structure J 180 can extend slightly into and engage the superior spinous process 5202 Accordingly, the spinous process engagement structures 1140, 1 ! 80 and the tethers ! 142, 1 182 can substantially prevent the adjustable interspinous process brace ! 100 from migrating with respect to the spinous processes

1200, 1202

Also, in a particular embodiment, the adjustable interspinous process brace 1 !00 can be movable between a retracted position, shown in FIG 1 1, and one or more extended positions, shown in FiG. 12. In the retracted position, a distance 1210 between the inferior spinous process bracket I US and the superior spinous process bracket 1 158 can be minimized. However, when spacers 1122, 1 132 are installed, or otherwise disposed, within the interior chambers 1 120, 1 130 of the inferior support posts 1 1 10.. 1 112, the distance 1210 between the inferior spinous process bracket 1 1 18 and the superior spinous process bracket 1 158 can be greater than when in the retracted position

Accordingly, a distractor can be used to increase the distance between the superior spinous process 1202 and the inferior spinous process 1200 and the adjustable interspinous process brace 1 100 can be adjusted to support the superior spinous process 1202 and the inferior spinous process 1200, e.g., by placing spacers 1 122, 1 132 into the interior chambers ! 120, 1130. After the adjustable interspinous process brace 1 100 is adjusted accordingly, the distractor cart be removed and the adjustable interspinous process brace

1 100 can support the superior spinous process 1202 and the inferior spinous process 1200 and substantially prevent the distance between the superior spinous process 1202 and the inferior spinous process 1200 from returning to a pre-distraction value.

Description of a Second Method of Treating a Spine

Referring to FICJ. 13, a method of treating a spine is shown and commences at block 1300. At block 1300, a patient can be secured in a prone position, e.g., on an operating table, At block 1302. the posterior spine can be exposed in order to expose adjacent spinous processes. Further, at block 1304, a surgical retractor system can be installed to keep a surgical field open.

Mov ing to block 1306, a superior vertebra and inferior vertebra can be distracted In a particular embodiment, the superior vertebra and inferior vertebra can be distracted using a distractor. At block 1308, a distance between the adjacent spinous processes can be measured Thereafter, at block 131 Q it i s deterroi ned whether the άi straction is correct, e.g., has the superior vertebra and inferior vertebral been distracted such that a distance between the adjacent spinous processes has reached a value thai a surgeon has deemed therapeutic. For example, the superior vertebra and interior vertebra can be distracted in order to reduce impingement on a nerve root

If the distraction is not correct, the method can return to block 1306 and the superior vertebra and inferior vertebra can be further distracted Conversely, if the distraction is correct, the method can move to block 1312 and one or more spaces can be installed within an adjustable interspinous process brace In a particular embodiment, the spacers can be elastic Further, the spacers can be spherically shaped, cube shaped, disc shaped., or a combination thereof.

At block 1314. the adjustable interspinous process brace can be installed between the adjacent spinous processes. Thereafter, at decision step 1316, it can be determined whether the adjustable interspinous process brace fits correctly into the space between the adjacent spinous processes. If not, the method proceed to block 1318 and the adjustable interspinous process brace can be removed from between the adjacent interspinous processes. ^' The method can then return to block 13 12 and one or more additional spacers can be installed within the adjustable interspinous process brace On the other hand, if the adjustable interspinous process brace fits correctly between the adjacent spinous processes, the method can proceed to block 1320.

At block 1320, the surgical area can be irrigated. At block 1322, the refractor system can be removed Further, at biock 1324, the surgical wound can be dosed The surgical wound can be closed by simply allowing the patient ^' s skin to close due to the elasticity of the skin. Alternatively,, the surgical wound can be closed using sutures, surgical staples, or any other suitable surgical technique well known in the art At block

! 326, postoperative care can be initiated. The method can end at state 1328

Conclusion

With the configuration of structure described above, the adjustable interspinous process brace provides a device that can be used to treat a spine and substantially alleviate or minimize one or more symptoms associated with disc degeneration, facet joint degeneration, or a combination thereof. For example, the adjustable interspinous process brace can installed between adjacent spinous processes in order to support the spinous processes and maintain them at or near a predetermined distance there between

The above-disclosed subject matter is to be considered illustrative, and not restrictive, and the appended claims are intended to cover all such modifications, enhancements, and other embodiments that fall within the true spirit and scope of the present invention. Thus, to the maximum extent allowed by law, the scope of the present invention is to be determined by the broadest permissible interpretation of the following claims and their equivalents, and shall not be restricted or limited by the foregoing detailed description.