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 Codes "HWC, KTT"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 10603295007708 1172-70-000 117270000 CANCELLOUS BONE SCREW 6.5mm x 70mm NA DEPUY ORTHOPAEDICS, INC.
2 10603295007692 1172-65-000 117265000 CANCELLOUS BONE SCREW 6.5mm x 65mm NA DEPUY ORTHOPAEDICS, INC.
3 10603295007685 1172-60-000 117260000 CANCELLOUS BONE SCREW 6.5mm x 60mm NA DEPUY ORTHOPAEDICS, INC.
4 10603295007678 1172-55-000 117255000 CANCELLOUS BONE SCREW 6.5mm x 55mm NA DEPUY ORTHOPAEDICS, INC.
5 10603295007661 1172-50-000 117250000 CANCELLOUS BONE SCREW 6.5mm x 50mm NA DEPUY ORTHOPAEDICS, INC.
6 10603295007654 1172-45-000 117245000 CANCELLOUS BONE SCREW 6.5mm x 45mm NA DEPUY ORTHOPAEDICS, INC.
7 10603295007647 1172-40-000 117240000 CANCELLOUS BONE SCREW 6.5mm x 40mm NA DEPUY ORTHOPAEDICS, INC.
8 10603295007630 1172-35-000 117235000 CANCELLOUS BONE SCREW 6.5mm x 35mm NA DEPUY ORTHOPAEDICS, INC.
9 10603295007623 1172-30-000 117230000 CANCELLOUS BONE SCREW 6.5mm x 30mm NA DEPUY ORTHOPAEDICS, INC.
10 10603295007616 1172-25-000 117225000 CANCELLOUS BONE SCREW 6.5mm x 25mm NA DEPUY ORTHOPAEDICS, INC.
11 10603295007609 1172-20-000 117220000 CANCELLOUS BONE SCREW 6.5mm x 20mm NA DEPUY ORTHOPAEDICS, INC.
12 10603295007593 1172-15-000 117215000 CANCELLOUS BONE SCREW 6.5mm x 15mm NA DEPUY ORTHOPAEDICS, INC.
13 10381780441380 MBAIMP MBAIMP MBA Implant Set MBA™ Titanium Subtalar Implant System ASCENSION ORTHOPEDICS, INC.
14 10381780257288 MBASET MBA™ Instrument Set (05-5000) MBA™ ASCENSION ORTHOPEDICS, INC.
15 10381780257271 KOMPSET Kompressor™ Instrument Set (21-5000) Kompressor™ ASCENSION ORTHOPEDICS, INC.
16 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.
17 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.
18 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.
19 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.
20 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.
21 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.
22 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.
23 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.
24 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.
25 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.
26 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.
27 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.
28 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.
29 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.
30 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.
31 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.
32 10381780125730 XFIX5RINGIMP XFIX5RINGIMP The Integra External Fixation System set consists of rings and footplates. These The Integra External Fixation System set consists of rings and footplates. These devices are used for stability and structure. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
33 10381780125723 XFIX4RCKRIMP XFIX4RCKRIMP The Integra External Fixation System set consists of rings, footplates, anterior The Integra External Fixation System set consists of rings, footplates, anterior cross bars, and a rockerbottom. These devices are used for stability and structure. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
34 10381780125716 XFIX2RODSIMP XFIX2RODSIMP The Integra External Fixation System set consists of struts, rods, and hex posts The Integra External Fixation System set consists of struts, rods, and hex posts. These devices are used for support in the construct. Plates and a universal joint are also included. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
35 10381780125709 XFIX1BOLTIMP XFIX1BOLTIMP The Integra External Fixation System set consists of wires, half-pins, nuts, and The Integra External Fixation System set consists of wires, half-pins, nuts, and bolts. Instruments are also included to aid in assembly. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
36 10381780125679 12225223 12225223 The Integra External Fixation System two-post bridge is manufactured from stainl The Integra External Fixation System two-post bridge is manufactured from stainless steel. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
37 10381780125662 12224143 12224143 The Integra External Fixation System half ring is used for stability and structu The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
38 10381780125655 12224141 12224141 The Integra External Fixation System 5/8 ring is used for stability and structur The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
39 10381780125648 12224133 12224133 The Integra External Fixation System half ring is used for stability and structu The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
40 10381780125631 12224132 12224132 The Integra External Fixation System full ring is used for stability and structu The Integra External Fixation System full ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
41 10381780125624 12224131 12224131 The Integra External Fixation System 5/8 ring is used for stability and structur The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
42 10381780125617 12224114 12224114 The Integra External Fixation System anterior half ring is used for stability an The Integra External Fixation System anterior half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
43 10381780125600 12224113 12224113 The Integra External Fixation System half ring is used for stability and structu The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
44 10381780125594 12224112 12224112 The Integra External Fixation System full ring is used for stability and structu The Integra External Fixation System full ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
45 10381780125587 12224111 12224111 The Integra External Fixation System 5/8 ring is used for stability and structur The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
46 10381780125570 12224110 12224110 The Integra External Fixation System footplate is used for stability and structu The Integra External Fixation System footplate is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
47 10381780125563 12225400 12225400 A rockerbottom is attached to the bottom of the external device so that the pati A rockerbottom is attached to the bottom of the external device so that the patient may stand on it if needed. It is manufactured from aluminum and silicone rubber. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
48 10381780125556 12225032 12225032 A crossbar is manufactured from stainless steel and aluminum. It may be attached A crossbar is manufactured from stainless steel and aluminum. It may be attached to the anterior ring for additional support. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
49 10381780125549 12225030 12225030 A crossbar is manufactured from stainless steel and aluminum. It may be attached A crossbar is manufactured from stainless steel and aluminum. It may be attached to the anterior ring for additional support. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.
50 10381780125532 12224124 12224124 The Integra External Fixation System anterior half ring is used for stability an The Integra External Fixation System anterior half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation. Integra® External Fixation System ASCENSION ORTHOPEDICS, INC.