| 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 | M896MAR0FUSE5CC1 | MAR0Fuse5cc | MAR0Fuse Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
| 2 | M896MAR0FUSE1CC1 | MAR0Fuse1cc | MAR0Fuse Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
| 3 | M896MAR0FUSE10CC1 | MAR0Fuse10cc | MAR0FUSE Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
| 4 | M896IQSPPP1100 | Paste Mix Plus | IQSP-PP-110 | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
| 5 | M896IQSPPP1050 | Paste Mix Plux | IQSP-PP-105 | Synthetic bone graft | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
| 6 | M896IQSPPP1020 | Paste Mix Plus | IQSP-PP-102 | Synthetic bone graft | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
| 7 | M896IQSPPP1010 | Paste Mix Plus | IQSP-PP-101 | Synthetic Bone Graft | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
| 8 | M896IQSPMX1500 | Matrix | IQSP-MX-150 | lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. | InQu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
| 9 | M896IQSPMX1250 | Matrix | IQSP-MX-125 | lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. | InQu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
| 10 | M896IQSPGR1300 | Granules | IQSP-GR-130 | lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. | InQu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
| 11 | 18257200121878 | 711015 | Osteoconductive Scaffold Strip, 15cc | Collage | ORTHOFIX INC. | |
| 12 | 18257200121861 | 711010 | Osteoconductive Scaffold Strip 10 cc | Collage | ORTHOFIX INC. | |
| 13 | 18257200115136 | 710015 | Collage Osteoconductive Scaffold Putty 15cc | Collage | ORTHOFIX INC. | |
| 14 | 18257200115129 | 710010 | Collage Osteoconductive Scaffold Putty 10 cc | Collage | ORTHOFIX INC. | |
| 15 | 18257200115112 | 710005 | Collage Osteoconductive Scaffold Putty, 5cc | Collage | ORTHOFIX INC. | |
| 16 | 15060155711499 | 910-010Z | 910-010Z | genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set insitu or placed in the bead mould mat provided to form beads for implantation. When injected the mixturesets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex.genex® Bone Graft Substitute is MR safe. | Genex Bone Graft Substitute | BIOCOMPOSITES LTD |
| 17 | 15060155711482 | 910-005Z | 910-005Z | genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set insitu or placed in the bead mould mat provided to form beads for implantation. When injected the mixturesets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex.genex® Bone Graft Substitute is MR safe. | Genex Bone Graft Substitute | BIOCOMPOSITES LTD |
| 18 | 15060155711475 | 910-003Z | 910-003Z | genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set in situ or placed in the bead mould mat provided to form beads for implantation. When injected the mixture sets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex. genex® Bone Graft Substitute is MR safe. | Genex Bone Graft Substitute | BIOCOMPOSITES LTD |
| 19 | 15060155711451 | 620-003 | 620-003 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
| 20 | 15060155711420 | 910-010 | 910-010 | Genex® Bone Graft Substitute is a simple to use synthetic resorbable material de Genex® Bone Graft Substitute is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form Genex® Bone Graft Substitute a hard but resorbable matrix. Genex® Bone Graft Substitute is supplied sterile. | Genex® | BIOCOMPOSITES LTD |
| 21 | 15060155711413 | 910-005 | 910-005 | Genex® Bone Graft Substitute is a simple to use synthetic resorbable material de Genex® Bone Graft Substitute is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form Genex® Bone Graft Substiute, a hard but resorbable matrix. Genex® Bone Graft Substitute is supplied sterile. | Genex® | BIOCOMPOSITES LTD |
| 22 | 15060155711055 | 640-005 | 640-005 | Stimulan® DS Calcium Sulfate Bone Void Filler is provided sterile for single pat Stimulan® DS Calcium Sulfate Bone Void Filler is provided sterile for single patient use. The kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together, the resultant paste is to be injected or digitally packed into open bone/gap to cure insitu. The biodegradable, radiopaque mixture is resorbed in approximately 30-60 days when used in accordance with the device labelling. Stimulan® is manufactured from synthetic implant grade calcium sulfate dihydrate (CaS04, 2H20) that resporbs and is replaced with bone during the healing process. Also as the bone void filler is biodegradable and biocompatible; it may be used at an infected site. | Stimulan® DS | BIOCOMPOSITES LTD |
| 23 | 15060155711048 | 620-020 | 620-020 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
| 24 | 15060155711031 | 620-010 | 620-010 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
| 25 | 15060155711024 | 620-005 | 620-005 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
| 26 | 15060155710966 | 980-005 | 980-005 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe.When injected the mixture sets to form geneX®; a hard but resorbable matrix. | geneX® ds | BIOCOMPOSITES LTD |
| 27 | 15060155710959 | 980-002 | 980-002 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe.When injected the mixture sets to form geneX®; a hard but resorbable matrix. | geneX® ds | BIOCOMPOSITES LTD |
| 28 | 15060155710188 | 920-010 | 920-010 | geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. | geneX® putty | BIOCOMPOSITES LTD |
| 29 | 15060155710171 | 920-005 | 920-005 | geneX® putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. | geneX® Putty | BIOCOMPOSITES LTD |
| 30 | 15060155710164 | 920-002 | 920-002 | geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. | geneX® putty | BIOCOMPOSITES LTD |
| 31 | 15060155710157 | 900-010 | 900-010 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX® a hard but resorbable matrix. geneX® is supplied sterile | geneX® | BIOCOMPOSITES LTD |
| 32 | 15060155710140 | 900-005 | 900-005 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX® a hard but resorbable matrix. geneX® is supplied sterile | geneX® | BIOCOMPOSITES LTD |
| 33 | 15060155710126 | 600-010 | 600-010 | STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be injected or digitally packed into open bone void/gap to set in situ or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Kit is manufactured from synthetic implant grade calcium sulfate dihydrate (CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Kit | BIOCOMPOSITES LTD |
| 34 | 15060155710119 | 600-005 | 600-005 | STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains STIMULAN® Kit - provided sterile for single patient use. STIMULAN® Kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be injected or digitally packed into open bone void/gap to set in situ or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Kit is manufactured from synthetic implant grade calcium sulfate dihydrate (CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Kit | BIOCOMPOSITES LTD |
| 35 | 15060155710096 | 600-30-s1 | 600-30-s1 | Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for sing Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for single patient use. The biodegradable, radiopaque pellets are resorbed in approximately 30-60 days when used in accordance with the device labelling. Calcium Sulfate Bone Filler is manufactured from medical grade calcium sulfate dihydrate (CaSO4 2H20) and stearic acid that resorbs and is replaced with bone during the healing process. Also as the bone void filler pellets are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Dispenser | BIOCOMPOSITES LTD |
| 36 | 15060155710072 | 600-48-010 | 600-48-010 | Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for sing Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for single patient use. The biodegradable, radiopaque pellets are resorbed in approximately 30-60 days when used in accordance with the device labelling. Calcium Sulfate Bone Filler is manufactured from medical grade calcium sulfate dihydrate (CaSO4 2H20) and stearic acid that resorbs and is replaced with bone during the healing process. Also as the bone void filler pellets are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Pellets | BIOCOMPOSITES LTD |
| 37 | 15060155710058 | 600-30-005 | 600-30-005 | Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for sing Stimulan® Calcium Sulfate Bone Void Filler pellets are provided sterile for single patient use. The biodegradable, radiopaque pellets are resorbed in approximately 30-60 days when used in accordance with the device labelling. Calcium Sulfate Bone Filler is manufactured from medical grade calcium sulfate dihydrate (CaSO4 2H20) and stearic acid that resorbs and is replaced with bone during the healing process. Also as the bone void filler pellets are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Pellets | BIOCOMPOSITES LTD |
| 38 | 15060155710034 | 800-010 | 800-010 | Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for single patient use. The biodegradable, radiopaque granules/blocks are resorbed in approximately 6-12 months when used in accordance with the device labelling. Biocomposites Tri-Calcium Phosphate Bone Graft Substitute is manufactured from medical grade Tri-Calcium Phosphate. Numerous bone graft operations are undertaken every year to repair bone defects caused by surgery, tumours, trauma, infections and other damage. Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is intended for use in clinical situations where the use of autologous grafts or other bone graft substitutes maybe undesirable, due either to the risk of associated infection or unavailability. Allogran-R® resorbs and is replaced with bone during the healing process. | Allogran-R® | BIOCOMPOSITES LTD |
| 39 | 15060155710027 | 800-005 | 800-005 | Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is provided sterile for single patient use. The biodegradable, radiopaque granules/blocks are resorbed in approximately 6-12 months when used in accordance with the device labelling. Biocomposites Tri-Calcium Phosphate Bone Graft Substitute is manufactured from medical grade Tri-Calcium Phosphate. Numerous bone graft operations are undertaken every year to repair bone defects caused by surgery, tumours, trauma, infections and other damage. Allogran-R® Tri-Calcium Phosphate Bone Graft Substitute is intended for use in clinical situations where the use of autologous grafts or other bone graft substitutes maybe undesirable, due either to the risk of associated infection or unavailability. Allogran-R® resorbs and is replaced with bone during the healing process. | Allogran-R® | BIOCOMPOSITES LTD |
| 40 | 14260418440796 | 200079 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 41 | 14260418440789 | 200078 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 42 | 14260418440772 | 200077 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 43 | 14260418440574 | 200057 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 44 | 14260418440567 | 200056 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 45 | 14260418440550 | 200055 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 46 | 14260418440543 | 200054 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® QD | ARTOSS GMBH | |
| 47 | 14260418440468 | 200046 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® SBX Putty | ARTOSS GMBH | |
| 48 | 14260418440451 | 200045 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® SBX Putty | ARTOSS GMBH | |
| 49 | 14260418440444 | 200044 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® SBX Putty | ARTOSS GMBH | |
| 50 | 14260418440437 | 200043 | Synthetic biodegradable bone graft substitute consisting of NanoBone® granulat Synthetic biodegradable bone graft substitute consisting of NanoBone® granulate (non-sintered nanocrystalline hydroxyapatite in a porous silica gel matrix) embedded in an aqueous gel | NanoBone® SBX Putty | ARTOSS GMBH |