No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00889024233638 | 42-5112-004-10 | 42-5112-004-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
2 | 00889024233621 | 42-5112-003-20 | 42-5112-003-20 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
3 | 00889024233614 | 42-5112-003-18 | 42-5112-003-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
4 | 00889024233607 | 42-5112-003-16 | 42-5112-003-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
5 | 00889024233591 | 42-5112-003-14 | 42-5112-003-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
6 | 00889024233584 | 42-5112-003-13 | 42-5112-003-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
7 | 00889024233577 | 42-5112-003-12 | 42-5112-003-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
8 | 00889024233560 | 42-5112-003-11 | 42-5112-003-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
9 | 00889024233553 | 42-5112-003-10 | 42-5112-003-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
10 | 00889024233546 | 42-5112-002-20 | 42-5112-002-20 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
11 | 00889024233539 | 42-5112-002-18 | 42-5112-002-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
12 | 00889024233522 | 42-5112-002-16 | 42-5112-002-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
13 | 00889024233515 | 42-5112-002-14 | 42-5112-002-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
14 | 00889024233508 | 42-5112-002-13 | 42-5112-002-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
15 | 00889024233492 | 42-5112-002-12 | 42-5112-002-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
16 | 00889024233485 | 42-5112-002-11 | 42-5112-002-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
17 | 00889024233478 | 42-5112-002-10 | 42-5112-002-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
18 | 00889024233461 | 42-5112-001-20 | 42-5112-001-20 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
19 | 00889024233454 | 42-5112-001-18 | 42-5112-001-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
20 | 00889024233447 | 42-5112-001-16 | 42-5112-001-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
21 | 00889024233430 | 42-5112-001-14 | 42-5112-001-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
22 | 00889024233423 | 42-5112-001-13 | 42-5112-001-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
23 | 00889024233416 | 42-5112-001-12 | 42-5112-001-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
24 | 00889024233409 | 42-5112-001-11 | 42-5112-001-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
25 | 00889024233393 | 42-5112-001-10 | 42-5112-001-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
26 | 00889024233386 | 42-5110-007-18 | 42-5110-007-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
27 | 00889024233379 | 42-5110-007-16 | 42-5110-007-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
28 | 00889024233362 | 42-5110-007-14 | 42-5110-007-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
29 | 00889024233355 | 42-5110-007-13 | 42-5110-007-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
30 | 00889024233348 | 42-5110-007-12 | 42-5110-007-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
31 | 00889024233331 | 42-5110-007-11 | 42-5110-007-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
32 | 00889024233324 | 42-5110-007-10 | 42-5110-007-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
33 | 00889024233317 | 42-5110-006-18 | 42-5110-006-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
34 | 00889024233300 | 42-5110-006-16 | 42-5110-006-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
35 | 00889024233294 | 42-5110-006-14 | 42-5110-006-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
36 | 00889024233287 | 42-5110-006-13 | 42-5110-006-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
37 | 00889024233270 | 42-5110-006-12 | 42-5110-006-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
38 | 00889024233263 | 42-5110-006-11 | 42-5110-006-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
39 | 00889024233256 | 42-5110-006-10 | 42-5110-006-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
40 | 00889024233249 | 42-5110-005-18 | 42-5110-005-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
41 | 00889024233232 | 42-5110-005-16 | 42-5110-005-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
42 | 00889024233225 | 42-5110-005-14 | 42-5110-005-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
43 | 00889024233218 | 42-5110-005-13 | 42-5110-005-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
44 | 00889024233201 | 42-5110-005-12 | 42-5110-005-12 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
45 | 00889024233195 | 42-5110-005-11 | 42-5110-005-11 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
46 | 00889024233188 | 42-5110-005-10 | 42-5110-005-10 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
47 | 00889024233171 | 42-5110-004-18 | 42-5110-004-18 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
48 | 00889024233164 | 42-5110-004-16 | 42-5110-004-16 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
49 | 00889024233157 | 42-5110-004-14 | 42-5110-004-14 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ | |
50 | 00889024233140 | 42-5110-004-13 | 42-5110-004-13 | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | PERSONA™ |
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 |