| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | M684EPT6514LWD1 | EPT6514LWD | EPT6514LWD | HWT | TEMPLATE | 1 | PS | |
| 2 | M684PNV036111 | PNV03611 | PNV03611 | JWH,MBH,OOG | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 3 | M684PHA062121 | PHA06212 | PHA06212 | LPH,LZO | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented | 2 | PROCOTYL | |
| 4 | M684KTIBTL2U1 | KTIBTL2U | KTIBTL2U | HWT | TEMPLATE | 1 | ADVANCE® | |
| 5 | M684KTTINP251 | KTTINP25 | KTTINP25 | HRY,JWH | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER,PROSTH PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | ADVANCE | |
| 6 | M684KTRLBF601 | KTRLBF60 | KTRLBF60 | HWT | TEMPLATE | 1 | ODYSSEY® | |
| 7 | M684KITLL1071 | KITLL107 | KITLL107 | HWT | TEMPLATE | 1 | ADVANCE® | |
| 8 | M684KIDT414L1 | KIDT414L | KIDT414L | HWT | TEMPLATE | 1 | ADVANCE® | |
| 9 | M684KIDT412R1 | KIDT412R | KIDT412R | HWT | TEMPLATE | 1 | ADVANCE® | |
| 10 | M684KFPCMR101 | KFPCMR10 | KFPCMR10 | HWT | TEMPLATE | 1 | ODYSSEY® | |
| 11 | M684ETRKN4SL1 | ETRKN4SL | ETRKN4SL | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | EVOLUTION® | |
| 12 | M684EAT4212L1 | EAT4212L | EAT4212L | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 13 | M684EFSAN1PR1 | EFSAN1PR | EFSAN1PR | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | EVOLUTION | |
| 14 | M684EAT7517R1 | EAT7517R | EAT7517R | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 15 | M684EAT6310R1 | EAT6310R | EAT6310R | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 16 | M684EAT5217R1 | EAT5217R | EAT5217R | HWT | TEMPLATE | 1 | EVOLUTION® | |
| 17 | M684EFXPNP4L1 | EFXPNP4L | EFXPNP4L | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | EVOLUTION | |
| 18 | M684E63043RL1 | E63043RL | E63043RL | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 19 | M684E63048RL1 | E63048RL | E63048RL | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 20 | M684E63042RL1 | E63042RL | E63042RL | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 21 | M684E17046821 | E1704682 | E1704682 | PBF | Orthopaedic surgical planning and instrument guides | 2 | Evolution Revision CCK System | |
| 22 | M684DNFLTRA11 | DNFLTRA1 | DNFLTRA1 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | DYNASTY® | |
| 23 | M684515618141 | 51561814 | 51561814 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | MicroPort | |
| 24 | M684400010581 | 40001058 | 40001058 | HWT | TEMPLATE | 1 | INTERSEAL® | |
| 25 | M6843304LJ501 | 3304LJ50 | 3304LJ50 | HWT | TEMPLATE | 1 | DYNASTY® | |
| 26 | M6843658XR151 | 3658XR15 | 3658XR15 | HWT | TEMPLATE | 1 | LINEAGE® | |
| 27 | M684333300201 | 33330020 | 33330020 | HWA | IMPACTOR | 1 | DYNASTY® | |
| 28 | M6843000AG011 | 3000AG01 | 3000AG01 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | INTERSEAL® | |
| 29 | M684188160521 | 18816052 | 18816052 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | Advantim | |
| 30 | M684184191141 | 18419114 | 18419114 | HWT | TEMPLATE | 1 | ORTHOLOC® | |
| 31 | M684180700421 | 18070042 | 18070042 | HWT | TEMPLATE | 1 | SLR | |
| 32 | M684184101331 | 18410133 | 18410133 | FZX | Guide, surgical, instrument | 1 | Advantium | |
| 33 | M684PNV040491 | PNV04049 | PNV04049 | OOG,MBH,JWH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SE Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 34 | M684PNV040481 | PNV04048 | PNV04048 | JWH,MBH,OOG | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 35 | M684PNV040471 | PNV04047 | PNV04047 | MBH,JWH,OOG | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 36 | M684PNV040461 | PNV04046 | PNV04046 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 37 | M684PNV040451 | PNV04045 | PNV04045 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 38 | M684PNV040441 | PNV04044 | PNV04044 | MBH,JWH,OOG | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 39 | M684PNV040431 | PNV04043 | PNV04043 | JWH,MBH,OOG | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 40 | M684PNV040421 | PNV04042 | PNV04042 | OOG,MBH,JWH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SE Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 41 | M684PNV040411 | PNV04041 | PNV04041 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 42 | M684PNV040401 | PNV04040 | PNV04040 | MBH,JWH,OOG | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system | 2 | PROPHECY | |
| 43 | M684PNV040391 | PNV04039 | PNV04039 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 44 | M684PNV040381 | PNV04038 | PNV04038 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 45 | M684PNV040371 | PNV04037 | PNV04037 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 46 | M684PNV040361 | PNV04036 | PNV04036 | JWH,OOG,MBH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 47 | M684PNV040351 | PNV04035 | PNV04035 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 48 | M684PNV040341 | PNV04034 | PNV04034 | OOG,JWH,MBH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEM Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 49 | M684PNV040331 | PNV04033 | PNV04033 | OOG,MBH,JWH | Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SE Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY | |
| 50 | M684PNV040321 | PNV04032 | PNV04032 | MBH,OOG,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PROPHECY |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 15060155711260 | 234-010-173 | 234-010-173 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 2 | 15060155711253 | 234-010-172 | 234-010-172 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 3 | 15060155711246 | 234-010-168 | 234-010-168 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 4 | 15060155711239 | 234-010-170 | 234-010-170 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 5 | 15060155711222 | 234-010-160 | 234-010-160 | The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorba The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorbable Poly (L-lactic) Acid and Calcium Phosphate which will be gradually resorbed into the body. this function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 6 | 15060155711215 | 3910-200-086 | 3910-200-086 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 7 | 15060155711208 | 3910-200-085 | 3910-200-085 | The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 8 | 15060155711192 | 3910-200-084 | 3910-200-084 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 9 | 15060155711185 | 3910-200-083 | 3910-200-083 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 10 | 15060155711178 | 3910-200-082 | 3910-200-082 | The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 11 | 15060155711161 | 3910-200-081 | 3910-200-081 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 12 | 15060155711154 | 3910-200-080 | 3910-200-080 | The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
| 13 | 15060155710652 | 160-135T | 160-135T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 14 | 15060155710645 | 160-130T | 160-130T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 15 | 15060155710621 | 160-935T | 160-935T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 16 | 15060155710614 | 160-930T | 160-930T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 17 | 15060155710607 | 160-925T | 160-925T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 18 | 15060155710584 | 160-830T | 160-830T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 19 | 15060155710577 | 160-825T | 160-825T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
| 20 | 15060155710546 | 160-725T | 160-725T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible and should not be used at an infected site. | Bilok® Screw | BIOCOMPOSITES LTD |
| 21 | 15060155710508 | 160-935ST | 160-935ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
| 22 | 15060155710492 | 160-930ST | 160-930ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
| 23 | 15060155710362 | 234-500-350 | 234-500-350 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
| 24 | 15060155710355 | 234-500-340 | 234-500-340 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
| 25 | 15060155710348 | 234-010-180 | 234-010-180 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 26 | 15060155710331 | 234-010-179 | 234-010-179 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 27 | 15060155710324 | 234-010-178 | 234-010-178 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 28 | 15060155710317 | 234-010-177 | 234-010-177 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 29 | 15060155710300 | 234-010-167 | 234-010-167 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 30 | 15060155710294 | 234-010-166 | 234-010-166 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 31 | 15060155710287 | 234-010-165 | 234-010-165 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 32 | 15060155710270 | 234-010-164 | 234-010-164 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 33 | 15060155710263 | 234-010-163 | 234-010-163 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 34 | 15060155710256 | 234-010-162 | 234-010-162 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 35 | 15060155710249 | 234-010-161 | 234-010-161 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
| 36 | 14061144348987 | GP001A.076.031.MH | GP001A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 37 | 14053613285541 | OC06D.076.032 | OC06D.076.032.STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
| 38 | 14053613285534 | OC907P.067.032 | OC907P.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 39 | 14053613285329 | GS905.050.032.M5 | GS905.050.032.STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 40 | 14053613285145 | 02-029-99-1004 | 02-029-99-1004 | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 41 | 14053613284780 | GP007.075.032.K4 | GP007.075.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 42 | 14053613284766 | GS901.033.032.K4 | GS901.033.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 43 | 14053613284391 | OC06Z.127.032 | OC06Z.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
| 44 | 14053613284384 | OC04N.127.032 | OC04N.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
| 45 | 14053613284377 | OC06D.067.032 | OC06D.067.032 STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
| 46 | 14053613284223 | GP007A.076.031 | GP007A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 47 | 14053613283837 | OC005.067.032 STE | OC005.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 48 | 14053613282625 | GP003A.027.030.M5 | GP003A.027.030 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 49 | 14053613282601 | OC002A.089.032 STE | OC002A.089.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
| 50 | 14053613282069 | GP005.067.032.M5 | GP005.067.032 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG |