Other products from "ZIMMER, INC."
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™
Other products with the same Product Code "HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M621OW30LBS26MM0 GM-500-26 OW3.0LBS-26MM osteo-WEDGE 3.0mm x 26mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 26mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 26mm Locking Bone Screw GRAMEDICA
2 M621OW30LBS24MM0 GM-500-24 OW3.0LBS-24MM osteo-WEDGE 3.0mm x 24mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 24mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 24mm Locking Bone Screw GRAMEDICA
3 M621OW30LBS22MM0 GM-500-22 OW3.0LBS-22MM osteo-WEDGE 3.0mm x 22mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 22mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 22mm Locking Bone Screw GRAMEDICA
4 M621OW30LBS20MM0 GM-500-20 OW3.0LBS-20MM osteo-WEDGE 3.0mm x 20mm Locking Bone Screw. For use with the osteo-WEDGE Openi osteo-WEDGE 3.0mm x 20mm Locking Bone Screw. For use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 20mm Locking Bone Screw GRAMEDICA
5 M621OW30LBS18MM0 GM-500-18 OW3.0LBS-18MM osteo-WEDGE 3.0mm x 18mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 18mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 18mm Locking Bone Screw GRAMEDICA
6 M621OW30LBS16MM0 GM-500-16 OW3.0LBS-16MM osteo-WEDGE 3.0mm x 16mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 16mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 16mm Locking Bone Screw GRAMEDICA
7 M621OW30LBS14MM0 GM-500-14 OW3.0LBS-14MM osteo-WEDGE 3.0mm x 14mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 14mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 14mm Locking Bone Screw GRAMEDICA
8 M621OW30LBS12MM0 GM-500-12 OW3.0LBS-12MM osteo-WEDGE 3.0mm x 12mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 12mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 12mm Locking Bone Screw GRAMEDICA
9 M621OW30LBS10MM0 GM-500-10 OW3.0LBS-10MM osteo-WEDGE 3.0mm x 10mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 10mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 10mm Locking Bone Screw GRAMEDICA
10 M621OW30LBS08MM0 GM-500-08 OW3.0LBS-08MM osteo-WEDGE 3.0mm x 08mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 3.0mm x 08mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 3.0mm x 08mm Locking Bone Screw GRAMEDICA
11 M621OW25LBS22MM0 GM-200-22 OW2.5LBS-22MM osteo-WEDGE 2.5mm x 22mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 22mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 22mm Locking Bone Screw GRAMEDICA
12 M621OW25LBS20MM0 GM-200-20 OW2.5LBS-20MM osteo-WEDGE 2.5mm x 20mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 20mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 20mm Locking Bone Screw GRAMEDICA
13 M621OW25LBS18MM0 GM-200-18 OW2.5LBS-18MM osteo-WEDGE 2.5mm x 18mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 18mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 18mm Locking Bone Screw GRAMEDICA
14 M621OW25LBS16MM0 GM-200-16 OW2.5LBS-16MM osteo-WEDGE 2.5mm x 16mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 16mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 16mm Locking Bone Screw GRAMEDICA
15 M621OW25LBS14MM0 GM-200-14 OW2.5LBS-14MM osteo-WEDGE 2.5mm x 14mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 14mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 14mm Locking Bone Screw GRAMEDICA
16 M621OW25LBS12MM0 GM-200-12 OW2.5LBS-12MM osteo-WEDGE 2.5mm x 12mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 12mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 12mm Locking Bone Screw GRAMEDICA
17 M621OW25LBS10MM0 GM-200-10 OW2.5LBS-10MM osteo-WEDGE 2.5mm x 10mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 10mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 10mm Locking Bone Screw GRAMEDICA
18 M621OW25LBS08MM0 GM-200-08 OW2.5LBS-08MM osteo-WEDGE 2.5mm x 08mm Locking Bone Screw. Non-sterile single use implant for osteo-WEDGE 2.5mm x 08mm Locking Bone Screw. Non-sterile single use implant for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE 2.5mm x 08mm Locking Bone Screw GRAMEDICA
19 M621OW24TT12MM0 GM-100-12 OW2.4TT-12MM osteo-WEDGE Temporary Tack, 2.4mm x 12mm. Non-sterile single use (disposable) a osteo-WEDGE Temporary Tack, 2.4mm x 12mm. Non-sterile single use (disposable) accessory for use with the osteo-WEDGE Opening Wedge Bone Locking Plate System. The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE Temporary Tack 2.4mm x 12mm GRAMEDICA
20 M621HYPINSTRAY0 HYP-INS-TRAY HYP-INS-TRAY HyProCure (reusable) Instrument Set. The instrument set contains six Trial Sizer HyProCure (reusable) Instrument Set. The instrument set contains six Trial Sizers (05mm thru 10mm), one Driver and three Guide Wires. For use with the HyProCure Sinus Tarsi Implant system. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Instrument Set GRAMEDICA
21 M621HYPIITS120 HYP II-TS-12 HYP II-TS-12 HyProCure II Trial Sizer 12 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 12 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Trial Sizer 12 GRAMEDICA
22 M621HYPIITS110 HYP II-TS-11 HYP II-TS-11 HyProCure II Trial Sizer 11 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 11 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion.. HyProCure II Trial Sizer 11 GRAMEDICA
23 M621HYPIITS100 HYP II-TS-10 HYP II-TS-10 HyProCure II Trial Sizer 10 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 10 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Trial Sizer 10 GRAMEDICA
24 M621HYPIITS090 HYP II-TS-09 HYP II-TS-09 HyProCure II Trial Sizer 09 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 09 instrument. For use with the HyProCure II Sinus Tarsi Implants. The HyProCure II (HYP II and HYP IIs) Sinus Tarsi Implant system is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Trial Sizer 09 GRAMEDICA
25 M621HYPIITS080 HYP II-TS-08 HYP II-TS-08 HyProCure II Trial Sizer 08 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 08 instrument. For use with the HyProCure II Sinus Tarsi Implants. The HyProCure II (HYP II and HYP IIs) Sinus Tarsi Implant system is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Trial Sizer 08 GRAMEDICA
26 M621HYPIITS070 HYP II-TS-07 HYP II-TS-07 HyPrHyProCure II Trial Sizer 07 instrument. For use with the HyProCure II Sinus HyPrHyProCure II Trial Sizer 07 instrument. For use with the HyProCure II Sinus Tarsi Implants. The HyProCure II (HYP II and HYP IIs) Sinus Tarsi Implant system is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Trial Sizer 07 GRAMEDICA
27 M621HYPIITS060 HYP II-TS-06 HYP II-TS-06 HyProCure II Trial Sizer 06 instrument. For use with the HyProCure II Sinus Tar HyProCure II Trial Sizer 06 instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Trial Sizer 06 GRAMEDICA
28 M621HYPIIPS0 HYPII-PS HYPII-PS HyProCure II Positioning Sleeve instrument. For use with the HyProCure II Sinus HyProCure II Positioning Sleeve instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Positioning Sleeve GRAMEDICA
29 M621HYPIIINSTRAY0 HYPII-INS-TRAY HYPII-INS-TRAY HyProCure II (reusable) Instrument Tray-Kit. The Instrument kit contains seven HyProCure II (reusable) Instrument Tray-Kit. The Instrument kit contains seven Trial Sizers (06mm thru 12mm) one Driver, one Positioning Sleeve and three Guide Wires). For use with the HyProCure II Sinus Tarsi Implants. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion HyProCure II Instrument Tray-Set GRAMEDICA
30 M621HYPII50 HYP II-5 HYP II-5 HyProCure II Driver instrument. For use with the HyProCure II Sinus Tarsi Impla HyProCure II Driver instrument. For use with the HyProCure II Sinus Tarsi Implant System. Indications: The HyProCure II (HYP II and HYP IIs) Implant is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Driver GRAMEDICA
31 M621HYPII120 HYP II-12 HYP II-12 HyProCure II Sinus Tarsi Implant Size 12. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 12. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 12 GRAMEDICA
32 M621HYPII110 HYP II-11 HYP II-11 HyProCure II Sinus Tarsi Implant Size 11. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 11. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 11 GRAMEDICA
33 M621HYPII100 HYP II-10 HYP II-10 HyProCure II Sinus Tarsi Implant Size 10. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 10. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 10 GRAMEDICA
34 M621HYPII090 HYP II-09 HYP II-09 HyProCure II Sinus Tarsi Implant Size 09. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 09. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 09 GRAMEDICA
35 M621HYPII080 HYP II-08 HYP II-08 HyProCure II Sinus Tarsi Implant Size 08. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 08. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 08 GRAMEDICA
36 M621HYPII070 HYP II-07 HYP II-07 HyProCure II Sinus Tarsi Implant Size 07. Indications: HyProCure II (HYP II a HyProCure II Sinus Tarsi Implant Size 07. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 07 GRAMEDICA
37 M621HYPII060 HYP II-06 HYP II-06 HyProCure II Sinus Tarsi Implant Size 06. Indications: HyProCure II (HYP II an HyProCure II Sinus Tarsi Implant Size 06. Indications: HyProCure II (HYP II and HYP IIs) is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. HyProCure II Sinus Tarsi Stent Size 06 GRAMEDICA
38 M621HYPGUIDEWIRES0 HYP-GuideWires HYP-GuideWires Guide Wire, a reusable instrument, for use with the HyProCure or HyProCure II Si Guide Wire, a reusable instrument, for use with the HyProCure or HyProCure II Sinus Tarsi Implant System. Indications: HyProCure is an implant stabilization device used in the treatment of hyperpronating instability of the hindfoot. The implant is designed to stabilize the talus to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus, while allowing normal talotarsal joint motion. Guide Wire GRAMEDICA
39 M621HYP100 HYP-10 HYP-10 HyProCure Sinus Tarsi Implant Size 10. Indications: HyProCure is a talotarsa HyProCure Sinus Tarsi Implant Size 10. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Size 10 GRAMEDICA
40 M621HYP090 HYP-09 HYP-09 HyProCure Sinus Tarsi Implant Size 09. Indications: HyProCure is a talotars HyProCure Sinus Tarsi Implant Size 09. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Size 09 GRAMEDICA
41 M621HYP080 HYP-08 HYP-08 HyProCure Sinus Tarsi Implant Size 08. Indications: HyProCure is a talotarsa HyProCure Sinus Tarsi Implant Size 08. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Size 08 GRAMEDICA
42 M621HYP070 HYP-07 HYP-07 HyProCure Sinus Tarsi Implant Size 07. Indications: HyProCure is a talotar HyProCure Sinus Tarsi Implant Size 07. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Size 07 GRAMEDICA
43 M621HYP060 HYP-06 HYP-06 HyProCure Sinus Tarsi Implant Size 06. Indications: HyProCure is a talotarsal HyProCure Sinus Tarsi Implant Size 06. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Size 06 GRAMEDICA
44 M621HYP050 HYP-05 HYP-05 HyProCure Sinus Tarsi Implant Size 05. Indications: HyProCure is a talotarsal HyProCure Sinus Tarsi Implant Size 05. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Size 05 GRAMEDICA
45 M621HD5FG0 HD-5-FG HD-5-FG HyProCure Driver. Reusable instrument, for use with the HyProCure Sinus Tarsi HyProCure Driver. Reusable instrument, for use with the HyProCure Sinus Tarsi Implant System. Indications: HyProCure is a talotarsal stabilization device used in the treatment of talotarsal dislocation and resulting sequela. The implant is designed to stabilize the talus on the tarsal mechanism to prevent excessive anterior, and/or medial, and/or plantarflexion of the talus on the tarsal mechanism, while allowing normal talotarsal joint motion. HyProCure Driver GRAMEDICA
46 M621GM504300 GM-504-30 GM-504-30 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE2 30 Degree Angulated Bone Plate Implant, Large GRAMEDICA
47 M621GM504270 GM-504-27 GM-504-27 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE2 27 Degree Angulated Bone Plate Implant, Large GRAMEDICA
48 M621GM504240 GM-504-24 GM-504-24 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE2 24 Degree Angulated Bone Plate Implant, Large GRAMEDICA
49 M621GM504210 GM-504-21 GM-504-21 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE2 21 Degree Angulated Bone Plate Implant, Large GRAMEDICA
50 M621GM504180 GM-504-18 GM-504-18 The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and tr The osteo-WEDGE Opening Wedge Bone Locking Plate System is used for adult and transitional adolescent (18 to 21 years old) patients for the purpose of stabilization and/or correction of angular deviations within an individual bone or in between two adjacent bones in the foot, such as opening wedge osteotomy for first metatarsal cuneiform joint deviations. osteo-WEDGE2 18 Degree Angulated Bone Plate Implant, Large GRAMEDICA