| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | M528G00003000 | G000-0300 | G000-0300 | Disposable Reamer 15mm, Glenoid | LXH | Orthopedic Manual Surgical Instrument | 1 | Glenoid GRS |
| 2 | M5288W950016W0 | 8W95-0016-W | 8W95-0016-W | Taper Post, 7.5mm Dia, Capitate, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 3 | M5288W153523W0 | 8W15-3523-W | 8W15-3523-W | 15mm Capitate Component, 35mm x 23mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 4 | M5288W153517W0 | 8W15-3517-W | 8W15-3517-W | 15mm Capitate Component, 35mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 5 | M5288W152223W0 | 8W15-2223-W | 8W15-2223-W | 15mm Capitate Component, 22mm x 23mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 6 | M5288W152217W0 | 8W15-2217-W | 8W15-2217-W | 15mm Capitate Component, 22mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 7 | M5288W123517W0 | 8W12-3517-W | 8W12-3517-W | 12mm Capitate Component, 35mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 8 | M5288W122217W0 | 8W12-2217-W | 8W12-2217-W | 12mm Capitate Component, 22mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 9 | M528P2051045W0 | P205-1045-W | P205-1045-W | Patella Comp, 20mm, 1.0x4.5mm, Anatomic CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 10 | M528PWR21155W0 | PWR2-1155-W | PWR2-1155-W | Femoral Component, Right, 11.5mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 11 | M528PWR21155A0 | PWR2-1155-A | PWR2-1155-A | Femoral Component, Right, 11.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 12 | M528PWR21005W0 | PWR2-1005-W | PWR2-1005-W | Femoral Component, Right, 10.0mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 13 | M528PWR21005A0 | PWR2-1005-A | PWR2-1005-A | Femoral Component, Right, 10.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 14 | M528PWR20855W0 | PWR2-0855-W | PWR2-0855-W | Femoral Component, Right, 8.5mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 15 | M528PWR20855A0 | PWR2-0855-A | PWR2-0855-A | Femoral Component, Right, 8.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 16 | M528PWR20705W0 | PWR2-0705-W | PWR2-0705-W | Femoral Component, Right, 7.0mm Offset, Kahuna,CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 17 | M528PWR20705A0 | PWR2-0705-A | PWR2-0705-A | Femoral Component, Right, 7.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 18 | M528PWL21155W0 | PWL2-1155-W | PWL2-1155-W | Femoral Component, Left, 11.5 mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 19 | M528PWL21155A0 | PWL2-1155-A | PWL2-1155-A | Femoral Component, Left, 11.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 20 | M528PWL21005W0 | PWL2-1005-W | PWL2-1005-W | Femoral Component, Left, 10.0mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 21 | M528PWL21005A0 | PWL2-1005-A | PWL2-1005-A | Femoral Component, Left, 10.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 22 | M528PWL20855W0 | PWL2-0855-W | PWL2-0855-W | Femoral Component, Left, 8.5mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 23 | M528PWL20855A0 | PWL2-0855-A | PWL2-0855-A | Femoral Component, Left, 8.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 24 | M528PWL20705W0 | PWL2-0705-W | PWL2-0705-W | Femoral Component, Left, 7.0mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 25 | M528PWL20705A0 | PWL2-0705-A | PWL2-0705-A | Femoral Component, Left, 7.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 26 | M528P2060045W0 | P206-0045-W | P206-0045-W | Patella Comp, 20mm x 4.5mm, Button CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 27 | M528P2060045A0 | P206-0045-A | P206-0045-A | Patella Comp, 20mm x 4.5mm, Button | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 28 | M528P2060040W0 | P206-0040-W | P206-0040-W | Patella Comp, 20mm x 4.0 mm, Button CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 29 | M528P2060040A0 | P206-0040-A | P206-0040-A | Patella Comp, 20mm x 4.0 mm, Button | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 30 | M528P2060035W0 | P206-0035-W | P206-0035-W | Patella Comp, Button, 20mm, 3.5mm x 3.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 31 | M528P2060035A0 | P206-0035-A | P206-0035-A | Patella Comp, Button, 20mm, 3.5mm x 3.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 32 | M528P2060030W0 | P206-0030-W | P206-0030-W | Patella Comp, Button, 20mm, 3.0mm x 3.0mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 33 | M528P2060030A0 | P206-0030-A | P206-0030-A | Patella Comp, Button, 20mm, 3.0mm x 3.0mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 34 | M528P2060025W0 | P206-0025-W | P206-0025-W | Patella Comp, Button, 20mm, 2.5mm x 2.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 35 | M528P2060025A0 | P206-0025-A | P206-0025-A | Patella Comp, Button, 20mm, 2.5mm x 2.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 36 | M528P2051045A0 | P205-1045-A | P205-1045-A | Patella Comp, 20mm, 1.0x4.5mm, Anatomic | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 37 | M528P2051040W0 | P205-1040-W | P205-1040-W | Patella Comp, 20mm, 1.0x4.0mm, Anatomic CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 38 | M528P2051040A0 | P205-1040-A | P205-1040-A | Patella Comp, 20mm, 1.0x4.0mm, Anatomic | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 39 | M528P2051035W0 | P205-1035-W | P205-1035-W | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 40 | M528P2051035A0 | P205-1035-A | P205-1035-A | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 41 | M528P2051030W0 | P205-1030-W | P205-1030-W | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.0mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 42 | M528P2051030A0 | P205-1030-A | P205-1030-A | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.0mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 43 | M528P2051025W0 | P205-1025-W | P205-1025-W | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 2.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 44 | M528P2051025A0 | P205-1025-A | P205-1025-A | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 2.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 45 | M528P2023530W0 | P202-3530-W | P202-3530-W | Patello-Femoral, Fem Comp, 3.5x3.0 CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 46 | M528P2023530A0 | P202-3530-A | P202-3530-A | Patello-Femoral, Fem Comp, 3.5x3.0 | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 47 | M528P2023525W0 | P202-3525-W | P202-3525-W | Patello-Femoral, Fem Comp, 3.5x2.5 CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 48 | M528P2023525A0 | P202-3525-A | P202-3525-A | Patello-Femoral, Fem Comp, 3.5x2.5 | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 49 | M528P2023520W0 | P202-3520-W | P202-3520-W | Patello-Femoral, Fem Comp, 3.5x2.0 CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 50 | M528P2023520A0 | P202-3520-A | P202-3520-A | Patello-Femoral, Fem Comp, 3.5x2.0 | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 81195401200786 | TSCD-35-1226S | 9011-00 | 3.0mm Diameter by 12-26mm Length | BONE-LOK SLX BI-Cortical Compression Device | INTERVENTIONAL SPINE, INC |
| 2 | 81195401199424 | TMCD-45-6070S | 9023-04 | 4.5mm Diameter x 60-70mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 3 | 81195401198748 | TMCD-45-5060S | 9023-03 | 4.5mm Diameter x 50-60mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 4 | 81195401197062 | TMCD-45-4050S | 9023-02 | 4.5mm Diameter x 40-50mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 5 | 81195401196386 | TMCD-45-3040S | 9023-01 | 4.5mm Diameter x -30-40mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 6 | 81195401195600 | TMCD-35-1520S | 9022-05 | 3.5mm Diameter x -15-20mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 7 | 81195401194924 | TMCD-35-2025S | 9022-04 | 3.5mm Diameter x 20-25mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 8 | 81195401193248 | TMCD-35-2530S | 9022-03 | 3.5mm Diameter x 25-30mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 9 | 81195401192562 | TMCD-35-4050S | 9022-02 | 3.5mm Diameter x 40-50mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 10 | 81195401191886 | TMCD-35-3040S | 9022-01 | 3.5mm Diameter x 30-40mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 11 | 81195401190100 | TACD-27-1222S | 9010-00 | 2.7mm Diameter by 12-22mm Length | BONE-LOK SLX BI-Cortical Compression Device | INTERVENTIONAL SPINE, INC |
| 12 | 81195401189524 | SMCD-45-6070S | 9009-04 | 4.5mm Diameter x 6070mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 13 | 81195401188848 | SMCD-45-5060S | 9009-03 | 4.5mm Diameter x 50-60mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 14 | 81195401187162 | SMCD-45-4050S | 9009-02 | 4.5mm Diameter x 40-50mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 15 | 81195401186486 | SMCD-45-3040S | 9009-01 | 4.5mm Diameter x 30-40mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 16 | 81195401185700 | SMCD-35-1520S | 9008-05 | 3.5mm Diameter x -15-20mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 17 | 81195401184024 | SMCD-35-2025S | 9008-04 | 3.5mm Diameter x -20-25mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 18 | 81195401183348 | SMCD-35-2530S | 9008-03 | 3.5mm Diameter x 25-30mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 19 | 81195401182662 | SMCD-35-4050S | 9008-02 | 3.5mm Diameter x 40-50mm Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 20 | 81195401181986 | SMCD-35-3040S | 9008-01 | 3.5mm Diameter x 30-40 Length | BONE-LOK MVP Cortical-Cancellous Compression Device | INTERVENTIONAL SPINE, INC |
| 21 | 81195401094248 | TLCD-73-120130S32 | 9019-06 | 7.3mm Diameter by 120-130mm (32) Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 22 | 81195401093562 | TLCD-73-110120S32 | 9019-05 | 7.3mm Diameter by 110-120mm (32) Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 23 | 81195401092886 | TLCD-73-100110S32 | 9019-04 | 7.3mm Diameter by 100-110mm (32) Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 24 | 81195401091100 | TLCD-73-90100S32 | 9019-03 | 7.3mm Diameter by 90-100mm (32) Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 25 | 81195401090424 | TLCD-73-8090S32 | 9019-02 | 7.3mm Diameter by 80-90mm (32) Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 26 | 81195401089848 | TLCD-73-7080S32 | 9019-01 | 7.3mm Diameter by 70-80mm (32) Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 27 | 81195401088162 | TLCD-73-120130S | 9015-06 | 7.3mm Diameter by 120-130mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 28 | 81195401087486 | TLCD-73-110120S | 9015-05 | 7.3mm Diameter by 110-120mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 29 | 81195401086700 | TLCD-73-100110S | 9015-04 | 7.3mm Diameter by 100-110mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 30 | 81195401085024 | TLCD-73-90100S | 9015-03 | 7.3mm Diameter by 90-100mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 31 | 81195401084348 | TLCD-73-8090S | 9015-02 | 7.3mm Diameter by 80-90mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 32 | 81195401083662 | TLCD-73-7080S | 9015-01 | 7.3mm Diameter by 70-80mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 33 | 81195401066900 | TLCD-73-6070S | 9017-03 | 7.3mm Diameter by 60-70mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 34 | 81195401065224 | TLCD-73-5060S | 9017-02 | 7.3mm Diameter by 50-60mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 35 | 81195401064548 | TLCD-73-4050S | 9017-01 | 7.3mm Diameter by 40-50mm Length | 7.3mm BONE-LOK Implant | INTERVENTIONAL SPINE, INC |
| 36 | 70721902805485 | 8004105 | BATTERY 8004105 BPD 5-PACK | TiMesh® | MEDTRONIC PS MEDICAL, INC. | |
| 37 | 50601557106556 | 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 |
| 38 | 50601557106488 | 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 |
| 39 | 50601557106242 | 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 |
| 40 | 50601557106174 | 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 |
| 41 | 50601557106006 | 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 |
| 42 | 50601557105870 | 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 |
| 43 | 50601557105702 | 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 |
| 44 | 50601557105498 | 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 |
| 45 | 50601557105016 | 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 |
| 46 | 50601557104958 | 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 |
| 47 | 37613327283601 | 52-91766 | 52-91766 | BONE SCREWS, CROSS-PIN, AUTO-PILOT | AUTO PILOT | STRYKER LEIBINGER GMBH & CO. KG |
| 48 | 37613327283595 | 52-91765 | 52-91765 | BONE SCREWS, CROSS-PIN, AUTO-PILOT | AUTO PILOT | STRYKER LEIBINGER GMBH & CO. KG |
| 49 | 37613327072618 | 690035 | 690035 | Kirschner Wire | NA | STRYKER TRAUMA SA |
| 50 | 37613327072601 | 390192 | 390192 | Kirschner Wire | NA | STRYKER TRAUMA SA |