Other products from "STRYKER CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 07613154111725 48552334 48552334 POLYAXIAL SCREW NKG,KWP Orthosis, cervical pedicle screw spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 OASYS
2 04546540680914 47112650 47112650 STRAIGHT ROD MNH,NKB,MNI Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, f Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINAL PEDICLE FIXATION 2 TRIO TRAUMA
3 04546540677747 486615160 486615160 VITALLIUM RAD ROD, WITH HEX NKB,KWP,KWQ,MNH,MNI Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXA Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
4 04546540645647 48824018 48824018 VARIABLE, SELF-DRILLING SCREW KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 AVIATOR
5 04546540645500 48814010 48814010 VARIABLE, SELF TAPPING SCREW KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 AVIATOR
6 04546540645357 48811246 48811246 TWO-LEVEL ANTERIOR PLATE KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 AVIATOR
7 04546540604859 486613602 486613602 VITALLIUM SPINAL ROD, WITH HEX MNI,NKB,KWQ,MNH,KWP ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degener ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
8 04546540591197 486613601 486613601 VITALLIUM SPINAL ROD KWQ,MNI,KWP,NKB,MNH APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATIO APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
9 04546540546609 486612645 486612645 MULTI-ANGLE SCREW CANNULATED NKB,MNH,MNI,KWP,KWQ Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spond Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
10 04546540546371 486614565 486614565 OFFSET CONNECTOR MNI,NKB,KWP,MNH,KWQ ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degener ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
11 04546540546364 486614560 486614560 AXIAL ROD TO ROD CONNECTOR KWP,NKB,KWQ,MNI,MNH APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
12 04546540546357 486614555 486614555 PARALLEL ROD TO ROD CONNECTOR MNI,MNH,NKB,KWQ,KWP ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,Or ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
13 04546540546340 486614550 486614550 AXIAL ROD TO ROD CONNECTOR KWQ,NKB,MNH,KWP,MNI APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixatio APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
14 04546540546326 486614320 486614320 LONG OFFSET CONNECTOR NEUTRAL KWQ,MNH,NKB,KWP,MNI APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spin APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
15 04546540546319 486614310 486614310 OFFSET CONNECTOR NEUTRAL MNH,KWQ,KWP,MNI,NKB Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVER Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease 2 RADIUS
16 04546540546296 486614300 486614300 SMALL ROD-ROD CONNECTOR MNH,KWQ,NKB,KWP,MNI Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVER Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
17 04546540546289 486614220 486614220 CROSS CONNECTOR KWP,KWQ,MNH,MNI,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease 2 RADIUS
18 04546540546272 486614219 486614219 CROSS CONNECTOR MNH,NKB,KWP,KWQ,MNI Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, f Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
19 04546540546265 486614218 486614218 CROSS CONNECTOR KWP,KWQ,NKB,MNH,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
20 04546540546258 486614217 486614217 CROSS CONNECTOR MNI,KWP,MNH,NKB,KWQ ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Ortho ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
21 04546540546241 486614216 486614216 CROSS CONNECTOR MNI,NKB,MNH,KWP,KWQ ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degener ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
22 04546540546203 486614140 486614140 CROSS CONNECTOR, VARIABLE M-A CURVED LONG MNH,NKB,KWP,KWQ,MNI Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, f Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
23 04546540546197 486614130 486614130 CROSS CONNECTOR, VARIABLE M-A CURVED MEDIUM MNH,KWP,NKB,MNI,KWQ Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAM Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
24 04546540546180 486614120 486614120 CROSS CONNECTOR, VARIABLE LONG KWP,MNH,MNI,NKB,KWQ APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
25 04546540546173 486614110 486614110 CROSS CONNECTOR, VARIABLE MEDIUM KWP,MNI,NKB,KWQ,MNH APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Ortho APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
26 04546540546166 486614100 486614100 CROSS CONNECTOR, VARIABLE SHORT KWQ,NKB,KWP,MNI,MNH APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixatio APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
27 04546540546159 486614036 486614036 CROSS CONNECTOR NKB,MNI,MNH,KWQ,KWP Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINA Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
28 04546540546142 486614034 486614034 CROSS CONNECTOR KWQ,KWP,MNH,MNI,NKB APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTE APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease 2 RADIUS
29 04546540546135 486614032 486614032 CROSS CONNECTOR MNI,MNH,NKB,KWQ,KWP ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,Or ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
30 04546540546128 486614030 486614030 CROSS CONNECTOR NKB,KWP,MNH,MNI,KWQ Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXA Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
31 04546540546111 486614028 486614028 CROSS CONNECTOR MNH,NKB,KWQ,MNI,KWP Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, f Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
32 04546540546104 486614026 486614026 CROSS CONNECTOR KWP,KWQ,MNI,MNH,NKB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEB APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease 2 RADIUS
33 04546540546098 486614024 486614024 CROSS CONNECTOR MNI,KWP,MNH,NKB,KWQ ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Ortho ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
34 04546540546081 486614022 486614022 CROSS CONNECTOR MNH,MNI,NKB,KWP,KWQ Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,Or Orthosis, spondylolisthesis spinal fixation,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
35 04546540545831 486613600 486613600 TITANIUM SPINAL ROD, WITH HEX KWP,MNI,KWQ,MNH,NKB,OSH APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,Pedicle screw spinal system, adolescent idiopathic scoliosis 2 RADIUS
36 04546540545428 486613054 486613054 TITANIUM SPINAL ROD, WITHOUT HEX KWQ,MNI,NKB,MNH,KWP APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATIO APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
37 04546540545411 486613053 486613053 TITANIUM SPINAL ROD, WITHOUT HEX MNI,KWP,MNH,NKB,KWQ ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Ortho ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
38 04546540545398 486613020 486613020 TITANIUM SPINAL ROD, WITHOUT HEX NKB,KWP,KWQ,OSH,MNI,MNH Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXA Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Pedicle screw spinal system, adolescent idiopathic scoliosis,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
39 04546540545381 486613010 486613010 TITANIUM SPINAL ROD, WITHOUT HEX OSH,MNI,KWP,NKB,MNH,KWQ Pedicle screw spinal system, adolescent idiopathic scoliosis,ORTHOSIS, SPINAL PE Pedicle screw spinal system, adolescent idiopathic scoliosis,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY 2 RADIUS
40 04546540545374 486613009 486613009 TITANIUM SPINAL ROD, WITHOUT HEX MNH,KWP,MNI,NKB,KWQ,OSH Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAM Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Pedicle screw spinal system, adolescent idiopathic scoliosis 2 RADIUS
41 04546540545367 486613008 486613008 TITANIUM SPINAL ROD, WITHOUT HEX MNH,KWQ,OSH,MNI,NKB,KWP Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVER Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Pedicle screw spinal system, adolescent idiopathic scoliosis,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
42 04546540545350 486613007 486613007 TITANIUM SPINAL ROD, WITHOUT HEX MNI,OSH,NKB,KWQ,MNH,KWP ORTHOSIS, SPINAL PEDICLE FIXATION,Pedicle screw spinal system, adolescent idiopa ORTHOSIS, SPINAL PEDICLE FIXATION,Pedicle screw spinal system, adolescent idiopathic scoliosis,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
43 04546540545343 486613006 486613006 TITANIUM SPINAL ROD, WITHOUT HEX MNI,KWQ,NKB,OSH,KWP,MNH ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BOD ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,Pedicle screw spinal system, adolescent idiopathic scoliosis,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
44 04546540545336 486613005 486613005 TITANIUM SPINAL ROD, WITHOUT HEX NKB,KWP,MNI,KWQ,MNH,OSH Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXA Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,Pedicle screw spinal system, adolescent idiopathic scoliosis 2 RADIUS
45 04546540545329 486613004 486613004 TITANIUM SPINAL ROD, WITHOUT HEX MNI,KWP,KWQ,MNH,NKB,OSH ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLI ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,Pedicle screw spinal system, adolescent idiopathic scoliosis 2 RADIUS
46 04546540545312 486613003 486613003 TITANIUM SPINAL ROD, WITHOUT HEX MNH,NKB,KWQ,OSH,MNI,KWP Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, f Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Pedicle screw spinal system, adolescent idiopathic scoliosis,ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
47 04546540545305 486613000 486613000 TITANIUM SPINAL ROD, WITHOUT HEX MNI,MNH,KWQ,KWP,NKB ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,AP ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for degenerative disc disease 2 RADIUS
48 04546540545190 486610000 486610000 LOCKING CAP MNI,KWQ,KWP,NKB,MNH ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BOD ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation 2 RADIUS
49 04546540545077 486610750 486610750 STANDARD SCREW KWQ,MNH,NKB,KWP,MNI APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spin APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spondylolisthesis spinal fixation,Orthosis, spinal pedicle fixation, for degenerative disc disease,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,ORTHOSIS, SPINAL PEDICLE FIXATION 2 RADIUS
50 04546540545060 486610745 486610745 STANDARD SCREW KWQ,MNI,NKB,MNH,KWP APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATIO APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,ORTHOSIS, SPINAL PEDICLE FIXATION,Orthosis, spinal pedicle fixation, for degenerative disc disease,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERLAMINAL 2 RADIUS
Other products with the same Product Codes "MQV, MBP"
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8 00817337000074 6000041 Tactoset is a synthetic, injectable, settable osteoconductive calcium phosphate Tactoset is a synthetic, injectable, settable osteoconductive calcium phosphate bone graft substitute material. Tactoset ANIKA THERAPEUTICS, INC.
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10 00816986020518 200X25X8 MM, 40 CC SGFS-040 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
11 00816986020501 100X25X8 MM, 20 CC SGFS-020 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
12 00816986020495 50X25X8 MM, 10 CC SGFS-010 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
13 00816986020488 25X25X8 MM, 5 CC SGFS-005 SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising b SIGNAFUSE Bioactive Bone Graft is a bioactive bone graft substitute comprising biphasic mineral granules and 45S5 bioactive glass suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. SIGNAFUSE Bioactive Bone Graft BIOVENTUS LLC
14 00816986020150 15g MSBG1500 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
15 00816986020143 7.5g MSBG0750 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
16 00816986020136 3.75g MSBG0375 Bioactive Bone Graft Putty UNITE Bioactive Bone Graft BIOVENTUS LLC
17 00816986020129 18cc OMP-18 OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules sus OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. OSTEOMATRIX+ BIOVENTUS LLC
18 00816986020112 9cc OMP-09 OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules sus OSTEOMATRIX+ is a bone graft substitute comprising biphasic mineral granules suspended in a porous type I collagen matrix. The device is provided sterile and is to be combined with autologous bone marrow aspirate prior to use to facilitate packing into bony defects. The device provides an osteoconductive scaffold that resorbs and guides host bone regeneration during the healing process. OSTEOMATRIX+ BIOVENTUS LLC
19 00816986020105 15g OF003 Bioactive Bone Graft Putty OSTEOFUSE BIOVENTUS LLC
20 00816986020099 7.5g OF002 Bioactive Bone Graft Putty OSTEOFUSE BIOVENTUS LLC
21 00816986020082 3.75g OF001 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. OSTEOFUSE BIOVENTUS LLC
22 00816986020037 IFBG100 IFBG100 INTERFACE is a synthetic bioactive bone graft for use in the repair of osseous d INTERFACE is a synthetic bioactive bone graft for use in the repair of osseous defects. It is supplied as irregular synthetic granules of bioactive glass (45S5 Bioglass), sized from 200 microns to 420 microns. When implanted in living tissue, the material undergoes a time dependent surface modification. The surface reaction results in the formation of a calcium phosphate layer, which is equivalent in composition and structure to the hydroxyapatite found in bone mineral. The biological apatite layer of the granules provides an osteoconductive scaffold for the generation of new osseous tissue. New bone infiltrates around the granules allowing the repair of the defect as the granules are absorbed. INTERFACE BIOVENTUS LLC
23 00816986020020 3.75g SGF-037 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. SIGNAFUSE BIOVENTUS LLC
24 00816986020013 7.5g SGF-075 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. SIGNAFUSE BIOVENTUS LLC
25 00816986020006 15g SGF-150 Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixtur Bioactive Bone Graft Putty is a synthetic bone void filler comprised of a mixture of calcium phosphate granules (CaP) and (45S5) bioactive glass granules suspended in a resorbable alkyleneoxide polymer (AOP) carrier that facilitates handling and delivery of the granule components. The device is supplied as putty, pre-loaded in a syringe applicator and packaged in a sterile barrier foil pouch. The device is provided sterile, for single use, in a variety of sizes. SIGNAFUSE BIOVENTUS LLC
26 00816125022229 RGT-50X25-05 RGT-50X25-05 R-GENIN is a bone void filler consisting of purified bovine collagen, hydroxyapa R-GENIN is a bone void filler consisting of purified bovine collagen, hydroxyapatite, tri-calcium phosphate, and demineralized bone matrix (DBM). The collagen component is biocompatible. After it is implanted, it resorbs and is later replaced by natural bone.R-GENIN is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine, and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. The bone graft can be mixed with autogenous blood prior to use at the physician's discretion. R-GENIN Strip BERKELEY ADVANCED BIOMATERIALS, LLC
27 00816125023868 ARM-TCP-BA-12 ARM-TCP-BA-12 HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix min HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.HA-TCP-Bioglass Sponge is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. HA-TCP-Bioglass Sponge must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. HA-TCP-Bioglass Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
28 00816125023851 ARM-TCP-10 ARM-TCP-10 HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I coll HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (60% hydroxyapatite - 40% tricalcium phosphate) resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.HA-TCP Sponge is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. HA-TCP Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
29 00816125023844 BF-10P BF-10P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (60% hydroxyapatite - 40% tricalcium phosphate) resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.Bi-Ostetic Foam Putty is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
30 00816125023837 BF-05P BF-05P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (60% hydroxyapatite - 40% tricalcium phosphate) resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.Bi-Ostetic Foam Putty is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
31 00816125023820 BF-02P BF-02P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (60% hydroxyapatite - 40% tricalcium phosphate) resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.Bi-Ostetic Foam Putty is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
32 00816125023813 BF-01P BF-01P Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Typ Bi-Ostetic Foam Putty is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (60% hydroxyapatite - 40% tricalcium phosphate) resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.Bi-Ostetic Foam Putty is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. Bi-Ostetic Foam Putty BERKELEY ADVANCED BIOMATERIALS, LLC
33 00816125023806 AA-10P AA-10P Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC
34 00816125023790 AA-05P AA-05P Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC
35 00816125023783 AA-01P AA-01P Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC
36 00816125023776 C10 SWE12 C10 SWE12 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
37 00816125023769 C10 SWE10 C10 SWE10 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
38 00816125023752 C10 SWE08 C10 SWE08 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
39 00816125023745 C10 SWE06 C10 SWE06 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Evans Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
40 00816125023738 C10 SWC08 C10 SWC08 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
41 00816125023721 C10 SWC07 C10 SWC07 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
42 00816125023714 C10 SWC06 C10 SWC06 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
43 00816125023707 C10 SWC05 C10 SWC05 Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and Tribio® DP Wedge is a bone void filler consisting of 60% hydroxyapatite (HA) and 40% beta-tri-calcium phosphate (TCP). These materials have been the topic of extensive clinical studies for several decades. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. After implantation, the device resorbs and is later replaced by natural bone. Tribio® DP Cotton Wedge BERKELEY ADVANCED BIOMATERIALS, LLC
44 00816125023691 AMWS-TCP-BA-12 AMWS-TCP-BA-12 HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix min HA-TCP-Bioglass Sponge is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.HA-TCP-Bioglass Sponge is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. HA-TCP-Bioglass Sponge must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. HA-TCP-Bioglass Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
45 00816125023684 AMWS-TCP-10 AMWS-TCP-10 HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I coll HA-TCP Sponge is a sterile bone graft composed of purified fibrillar Type I collagen and Bi-Ostetic (60% hydroxyapatite - 40% tricalcium phosphate) resorbable granules. This device is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.HA-TCP Sponge is indicated for use in bony voids or gaps that are not intrinsic to the stability of the bony structure. The product should be gently packed into bony voids or gaps of the skeletal system (i.e., the extremities, posterolateral spine and pelvis). These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone. The product provides a bone void filler that resorbs and is replaced by the growth of new bone during the healing process. In weight bearing situations, the graft is to be used in conjunction with internal or external fixation devices. The fracture defect treated should not exceed 30 ml. HA-TCP Sponge BERKELEY ADVANCED BIOMATERIALS, LLC
46 00816125023677 OB-10D OB-10D OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compoun OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, OsteoBoost Select resorbs and is later replaced by natural bone. It provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.OsteoBoost Select is an osteoconductive putty that is intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium.The putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs. OsteoBoost Select 10cc BERKELEY ADVANCED BIOMATERIALS, LLC
47 00816125023660 OB-05D OB-05D OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compoun OsteoBoost Select is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, OsteoBoost Select resorbs and is later replaced by natural bone. It provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.OsteoBoost Select is an osteoconductive putty that is intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium.The putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs. OsteoBoost Select 5cc BERKELEY ADVANCED BIOMATERIALS, LLC
48 00816125023653 M80 SB008 M80 SB008 Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralize Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible. The 45S5 glass particles are bioactive. The device is available in the form of granules, strips, and putty. The composition of the granules is 60 wt% HA and 40 wt% TCP. The amount of 45S5 granules in the graft is 20 wt%. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. This apatite layer on the 45S5 granules and hydroxyapatite-tri-calcium phosphate granules provide an osteoconductive scaffold onto which the patient’s new bone will grow. During healing, the graft particulate is absorbed and remodeled into new bone. Tribio™ Implant, 7.5mm x 40mm BERKELEY ADVANCED BIOMATERIALS, LLC
49 00816125023646 M80 SB006 M80 SB006 Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralize Tribio™ Implant is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible. The 45S5 glass particles are bioactive. The device is available in the form of granules, strips, and putty. The composition of the granules is 60 wt% HA and 40 wt% TCP. The amount of 45S5 granules in the graft is 20 wt%. The device provides a scaffold around which new bone can grow. A series of surface reactions on the particles results in the formation of a calcium phosphate layer that is substantially equivalent in composition and structure to the hydroxyapatite found in bone mineral. This apatite layer on the 45S5 granules and hydroxyapatite-tri-calcium phosphate granules provide an osteoconductive scaffold onto which the patient’s new bone will grow. During healing, the graft particulate is absorbed and remodeled into new bone. Tribio™ Implant, 5.5mm x 40mm BERKELEY ADVANCED BIOMATERIALS, LLC
50 00816125023639 AA1-100X25-12 AA1-100X25-12 Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen m Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive.Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine. Bi-Ostetic Bioactive Glass Foam BERKELEY ADVANCED BIOMATERIALS, LLC