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 | 10705034341903 | AC020 | AC020 | BREMER HIFIX HALO SKULL PIN SKULL PIN | BREMER HIFIX | DEPUY SPINE, LLC |
2 | 10705034034614 | 175704010 | 175704010 | DISCOVERY SCREW SYSTEM WASHER | DISCOVERY | DEPUY SPINE, LLC |
3 | 10705034009131 | 22261935 | 22261935 | VSP SPINE SYSTEM BONE SCREW STANDARD 4.75 x 35mm | VSP | DEPUY SPINE, LLC |
4 | 10603295007708 | 1172-70-000 | 117270000 | CANCELLOUS BONE SCREW 6.5mm x 70mm | NA | DEPUY ORTHOPAEDICS, INC. |
5 | 10603295007692 | 1172-65-000 | 117265000 | CANCELLOUS BONE SCREW 6.5mm x 65mm | NA | DEPUY ORTHOPAEDICS, INC. |
6 | 10603295007685 | 1172-60-000 | 117260000 | CANCELLOUS BONE SCREW 6.5mm x 60mm | NA | DEPUY ORTHOPAEDICS, INC. |
7 | 10603295007678 | 1172-55-000 | 117255000 | CANCELLOUS BONE SCREW 6.5mm x 55mm | NA | DEPUY ORTHOPAEDICS, INC. |
8 | 10603295007661 | 1172-50-000 | 117250000 | CANCELLOUS BONE SCREW 6.5mm x 50mm | NA | DEPUY ORTHOPAEDICS, INC. |
9 | 10603295007654 | 1172-45-000 | 117245000 | CANCELLOUS BONE SCREW 6.5mm x 45mm | NA | DEPUY ORTHOPAEDICS, INC. |
10 | 10603295007647 | 1172-40-000 | 117240000 | CANCELLOUS BONE SCREW 6.5mm x 40mm | NA | DEPUY ORTHOPAEDICS, INC. |
11 | 10603295007630 | 1172-35-000 | 117235000 | CANCELLOUS BONE SCREW 6.5mm x 35mm | NA | DEPUY ORTHOPAEDICS, INC. |
12 | 10603295007623 | 1172-30-000 | 117230000 | CANCELLOUS BONE SCREW 6.5mm x 30mm | NA | DEPUY ORTHOPAEDICS, INC. |
13 | 10603295007616 | 1172-25-000 | 117225000 | CANCELLOUS BONE SCREW 6.5mm x 25mm | NA | DEPUY ORTHOPAEDICS, INC. |
14 | 10603295007609 | 1172-20-000 | 117220000 | CANCELLOUS BONE SCREW 6.5mm x 20mm | NA | DEPUY ORTHOPAEDICS, INC. |
15 | 10603295007593 | 1172-15-000 | 117215000 | CANCELLOUS BONE SCREW 6.5mm x 15mm | NA | DEPUY ORTHOPAEDICS, INC. |
16 | 10381780441380 | MBAIMP | MBAIMP | MBA Implant Set | MBA™ Titanium Subtalar Implant System | ASCENSION ORTHOPEDICS, INC. |
17 | 10381780257288 | MBASET | MBA™ Instrument Set (05-5000) | MBA™ | ASCENSION ORTHOPEDICS, INC. | |
18 | 10381780257271 | KOMPSET | Kompressor™ Instrument Set (21-5000) | Kompressor™ | ASCENSION ORTHOPEDICS, INC. | |
19 | 10381780237686 | TRL-1006-C06 | The Integra Titanium Bone Wedges are a series of wedge-shaped devices intended t The Integra Titanium Bone Wedges are a series of wedge-shaped devices intended to be used for angular correction of small bones in the ankle and foot. The Integra Titanium Bone Wedges are constructed from commercially pure titanium formed into a cancellous-like structure. Trial Cotton 20 X 6.5 | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
20 | 10381780237679 | TRL-1006-C05 | The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
21 | 10381780237662 | TRL-1006-C04 | The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
22 | 10381780237655 | TRL-1006-C03 | The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
23 | 10381780237648 | TRL-1006-C02 | The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
24 | 10381780237631 | TRL-1006-C01 | The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is co The Integra® Titanium Cotton Wedge Trials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
25 | 10381780237624 | TRL-1006-L09 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
26 | 10381780237617 | TRL-1006-L08 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
27 | 10381780237600 | TRL-1006-L07 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
28 | 10381780237594 | TRL-1006-L06 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
29 | 10381780237587 | TRL-1006-L05 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
30 | 10381780237570 | TRL-1006-L04 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
31 | 10381780237563 | TRL-1006-L03 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
32 | 10381780237556 | TRL-1006-L02 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
33 | 10381780237549 | TRL-1006-L01 | The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congr The Integra® Titanium Bone WedgeTrials are inserted until the footprint is congruent to the dimensions of the osteotomy surface, and the desired amount of correction is achieved. The trial is to confirm that the implanted wedge will be congruent with the osteotomy surface to provide the most optimal site for ingrowth of bone into the wedge. | TiWedge™ | ASCENSION ORTHOPEDICS, INC. | |
34 | 10381780237471 | TIWEDGEINSTP | The Integra Titanium Bone Wedge is intended to be used for internal bone fixatio The Integra Titanium Bone Wedge is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot. This set includes LCL trials and cotton trials to evaluate proper size and fit of the implants. A wedge inserter and tamp are also included for assistance. | TiWedgeTM | ASCENSION ORTHOPEDICS, INC. | |
35 | 10381780124948 | TBW-1006-2065 | TBW-1006-2065 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
36 | 10381780124931 | TBW-1006-2055 | TBW-1006-2055 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
37 | 10381780124924 | TBW-1006-2045 | TBW-1006-2045 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
38 | 10381780124917 | TBW-1006-1665 | TBW-1006-1665 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
39 | 10381780124900 | TBW-1006-1655 | TBW-1006-1655 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
40 | 10381780124894 | TBW-1006-1645 | TBW-1006-1645 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
41 | 10381780124887 | TBW-1006-LG12 | TBW-1006-LG12 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
42 | 10381780124870 | TBW-1006-LG10 | TBW-1006-LG10 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
43 | 10381780124863 | TBW-1006-LG8 | TBW-1006-LG8 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
44 | 10381780124856 | TBW-1006-MD12 | TBW-1006-MD12 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
45 | 10381780124849 | TBW-1006-MD10 | TBW-1006-MD10 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
46 | 10381780124832 | TBW-1006-MD8 | TBW-1006-MD8 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
47 | 10381780124825 | TBW-1006-SM12 | TBW-1006-SM12 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
48 | 10381780124818 | TBW-1006-SM10 | TBW-1006-SM10 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
49 | 10381780124801 | TBW-1006-SM8 | TBW-1006-SM8 | The Integra® Titanium Bone Wedges are intended to be used for internal bone fixa The Integra® Titanium Bone Wedges are intended to be used for internal bone fixation for bone fracturesor osteotomies in the ankle and foot | Integra® Titanium Bone Wedge System | ASCENSION ORTHOPEDICS, INC. |
50 | 10381780123064 | CSS500000670WT | CSS500000670WT | The washer is used in conjunction with the Capture High Torque Screw System. | CAPTURE™ High Torque Screw System | ASCENSION ORTHOPEDICS, INC. |