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 |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00865179000073 | IN012 | IQSP-PP-101 | 1.25cc Paste Mix Plus | InQu | ISTO TECHNOLOGIES INC |
2 | 00865179000066 | IN010 | IQSP-PP-102 | 2.5cc Paste Mix Plus | InQu | ISTO TECHNOLOGIES INC |
3 | 00865179000059 | IN009 | IQSP-PP-105 | 5cc Paste Mix Plus | InQu | ISTO TECHNOLOGIES INC |
4 | 00865179000042 | IN008 | IQSP-PP-110 | 10cc Paste Mix Plus | InQu | ISTO TECHNOLOGIES INC |
5 | 00865179000035 | IN007 | IQSP-MX-125 | 5x5cm Matrix | InQu | ISTO TECHNOLOGIES INC |
6 | 00865179000028 | IN006 | IQSP-MX-150 | 5x10cm Matrix | InQu | ISTO TECHNOLOGIES INC |
7 | 00865179000011 | IN002 | IQSP-GR-110 | 10cc Granules | InQu | ISTO TECHNOLOGIES INC |
8 | 00865179000004 | IN001 | IQSP-GR-130 | 30cc Granules | InQu | ISTO TECHNOLOGIES INC |
9 | 00863787000478 | NGC10X | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
10 | 00863787000461 | NGC05X | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
11 | 00863787000454 | NGC025X | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
12 | 00863787000430 | NGC15 | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
13 | 00863787000423 | NGC10 | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
14 | 00863787000416 | NGC05 | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
15 | 00863787000409 | NGC025 | NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system. | NovoGro Putty | OSTEONOVUS, INC. | |
16 | 00862835000477 | 50-003 | 50-003 | Bone Void Filler Kit, 3cc | Synthecure | AUSTIN MEDICAL VENTURES INC. |
17 | 00862835000453 | 50-020 | 50-020 | Bone Void Filler Kit, 20cc | Synthecure | AUSTIN MEDICAL VENTURES INC. |
18 | 00862835000446 | 50-005 | 50-005 | Bone Void Filler Kit, 5cc | Synthecure | AUSTIN MEDICAL VENTURES INC. |
19 | 00862835000439 | 50-010 | 50-010 | Bone Void Filler Kit, 10cc | Synthecure | AUSTIN MEDICAL VENTURES INC. |
20 | 00862835000422 | 20-150 | 20-150 | Calcium Sulfate Bone Void Filler, Large | Synthecure | AUSTIN MEDICAL VENTURES INC. |
21 | 00862835000415 | 20-125 | 20-125 | Calcium Sulfate Bone Void Filler, Medium | Synthecure | AUSTIN MEDICAL VENTURES INC. |
22 | 00862835000408 | 20-112 | 20-112 | Calcium Sulfate Bone Void Filler, Small | Synthecure | AUSTIN MEDICAL VENTURES INC. |
23 | 00858686006096 | 100x25x7mm | ASI209-20 | Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intend Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intended for implantation | NanoFUSE Bioactive Strip | AMEND SURGICAL, INC. |
24 | 00858686006089 | 50x25x7mm | ASI209-10 | Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intend Bone void filler comprised of 45S5 bioactive glass and a gelatin carrier, intended for implantation | NanoFUSE Bioactive Strip | AMEND SURGICAL, INC. |
25 | 00858686006072 | BGP001-10 | BGP001-10 | Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser | Bio V BP Bioactive Glass with DBM Putty | AMEND SURGICAL, INC. |
26 | 00858686006065 | BGP001-05 | BGP001-05 | Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser | Bio V BP Bioactive Glass with DBM Putty - 5.0 cc | AMEND SURGICAL, INC. |
27 | 00858686006058 | BGP001-02 | BGP001-02 | Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser | Bio V BP Bioactive Glass with DBM Putty - 2.0 cc | AMEND SURGICAL, INC. |
28 | 00858686006041 | BGP001-01 | BGP001-01 | Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser | Bio V BP Bioactive Glass with DBM Putty | AMEND SURGICAL, INC. |
29 | 00858686006034 | NAN109-01 | NAN109-01 | Synthetic bone void filler containing DBM for orthopedic applications, provided Synthetic bone void filler containing DBM for orthopedic applications, provided in a syringe dispenser | NanoFuse Bioactive Matrix - 1.0 cc | AMEND SURGICAL, INC. |
30 | 00858686006027 | NAN109-10 | NAN109-10 | Synthetic bone void filler containing DBM for orthopedic applications | NanoFuse Bioactive Matrix - 10.0 cc | AMEND SURGICAL, INC. |
31 | 00858686006010 | NAN109-05 | NAN109-05 | Synthetic bone void filler containing DBM for orthopedic applications | NanoFuse Bioactive Matrix - 5.0 cc | AMEND SURGICAL, INC. |
32 | 00858686006003 | NAN109-02 | NAN109-02 | Synthetic bone void filler containing DBM for orthopedic applications | NanoFuse Bioactive Matrix - 2.0 cc | AMEND SURGICAL, INC. |
33 | 00858418003997 | BA42-501005 | BA42-501005 | STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collage STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device, formulated as a block (strip), is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.STRATOFUSE 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 30ml. | STRATOFUSE Strip | BERKELEY ADVANCED BIOMATERIALS, LLC |
34 | 00858418003980 | BA41-501005 | BA41-501005 | STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collage STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device, formulated as a block (strip), is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.STRATOFUSE 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 30ml. | STRATOFUSE Strip | BERKELEY ADVANCED BIOMATERIALS, LLC |
35 | 00858418003973 | BA41-501002 | BA41-501002 | STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collage STRATOFUSE is a sterile bone graft composed of purified fibrillar type I collagen and 60% hydroxyapatite - 40% tricalcium phosphate resorbable granules. This device, formulated as a block (strip), is safe and has excellent biocompatibility. After it is implanted, the graft resorbs and is later replaced by natural bone.STRATOFUSE 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 30ml. | STRATOFUSE Strip | BERKELEY ADVANCED BIOMATERIALS, LLC |
36 | 00858418003966 | SBiO-XYZ400606P | SBiO-XYZ400606P | SeaSpine Bi-Ostetic Cancellous Blocks is a mixture with a nominal composition of SeaSpine Bi-Ostetic Cancellous Blocks is a mixture with a nominal composition of 60% hydroxyapatite and 40% beta-tri-calcium phosphate. SeaSpine Bi-Ostetic Cancellous Blocks is safe and has excellent biocompatibility. After it is implanted, the implant resorbs and is later replaced by natural bone. SeaSpine Bi-Ostetic Cancellous Blocks is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.SeaSpine Bi-Ostetic Cancellous Blocks is an osteoconductive bone substitute shaped as blocks that are 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 blocks may be pressed into the void or into the surgical site by hand. The SeaSpine Bi-Ostetic Cancellous Blocks provide void filling material that acts as a temporary support medium. The blocks are not intended to provide structural support during the healing process. The implant is radio-opaque. SeaSpine Bi-Ostetic Cancellous Blocks is biocompatible and resorbs in the body as bone ingrowth occurs. | SeaSpine Bi-Ostetic Cancellous Block, 40x6x6mm | BERKELEY ADVANCED BIOMATERIALS, LLC |
37 | 00858418003959 | PCK-10 | PCK-10 | The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that all The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that allows the physician to mold bone putty into beads. | Putty Convenience Kit, 10cc | BERKELEY ADVANCED BIOMATERIALS, LLC |
38 | 00858418003942 | PCK-05 | PCK-05 | The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that all The Putty Convenience Kit (PCK) is a flexible polymer mat with cavities that allows the physician to mold bone putty into beads. | Putty Convenience Kit, 5cc | BERKELEY ADVANCED BIOMATERIALS, LLC |
39 | 00858418003935 | EBF1-100X25-15 | EBF1-100X25-15 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
40 | 00858418003928 | EBF1-100X25-10 | EBF1-100X25-10 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
41 | 00858418003911 | EBF1-90X22-07 | EBF1-90X22-07 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
42 | 00858418003904 | EBF1-90X22-10 | EBF1-90X22-10 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
43 | 00858418003898 | EBF2-50X25-10 | EBF2-50X25-10 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
44 | 00858418003881 | EBF2-50X10-05 | EBF2-50X10-05 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
45 | 00858418003874 | EBF1-50X10-02 | EBF1-50X10-02 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
46 | 00858418003867 | EBF2-50X10-02 | EBF2-50X10-02 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
47 | 00858418003850 | EBF1-50X10-01 | EBF1-50X10-01 | EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen EvoGraft is a sterile bone graft composed of purified fibrillar Type I collagen and 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.EvoGraft 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. | EvoGraft | BERKELEY ADVANCED BIOMATERIALS, LLC |
48 | 00858418003843 | CemO-DZ1040P | CemO-DZ1040P | Cem-Ostetic is a bio-engineered mixture of calcium-based inorganic compounds. Af Cem-Ostetic is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, Cem-Ostetic resorbs and is later replaced by natural bone. Cem-Ostetic is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.Cem-Ostetic is an osteoconductive bone substitute shaped as blocks (cylinders) that are 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 blocks (cylinders) may be pressed into the void or into the surgical site by hand. The Cem-Ostetic blocks (cylinders) provide void filling material that acts as a temporary support medium. The blocks (cylinders) are not intended to provide structural support during the healing process. The implant is radio-opaque. Cem-Ostetic is biocompatible and resorbs in the body as bone ingrowth occurs. | Cem-Ostetic Cylinder | BERKELEY ADVANCED BIOMATERIALS, LLC |
49 | 00858418003836 | CemO-30P | CemO-30P | Cem-Ostetic is a bio-engineered mixture of calcium-based inorganic compounds. Af Cem-Ostetic is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, Cem-Ostetic resorbs and is later replaced by natural bone. Cem-Ostetic is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.Cem-Ostetic 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. | Cem-Ostetic Putty | BERKELEY ADVANCED BIOMATERIALS, LLC |
50 | 00858418003829 | CemO-00G | CemO-00G | Cem-Ostetic is a bio-engineered mixture of calcium-based inorganic compounds. Af Cem-Ostetic is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, Cem-Ostetic resorbs and is later replaced by natural bone. Cem-Ostetic is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission.Cem-Ostetic is an osteoconductive bone substitute shaped as granules that are 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 granules may be pressed into the void or into the surgical site by hand. The Cem-Ostetic granules provide void filling material that acts as a temporary support medium. The granules are not intended to provide structural support during the healing process. The implant is radio-opaque. Cem-Ostetic is biocompatible and resorbs in the body as bone ingrowth occurs. | Cem-Ostetic Granules | BERKELEY ADVANCED BIOMATERIALS, LLC |