Other products from "PROVIDENCE MEDICAL TECHNOLOGY, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00852776006379 PD-31-613 PD-31-613 CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heigh CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only. OVE Intervertebral Fusion Device With Integrated Fixation, Cervical 2 CAVUX™ Cervical Cage-L 10x14x17mm
2 00852776006324 PD-31-201 CAVUX Cervical Cage is indicated for use in skeletally mature patients with dege CAVUX Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX™ Cervical Cage-B 5mm
3 00852776006294 PD-31-604 PD-31-604 CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with de CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX™ Cervical Cage-L 10x12x15mm 7 deg
4 00852776006027 PD-32-301 PD-32-301 The ALLY Bone Screw is a single-use implant made of titanium alloy and used in b The ALLY Bone Screw is a single-use implant made of titanium alloy and used in bone reconstruction, osteotomy, arthrodesis, join fusion, fracture repair and fixation appropriate for the size of the device. HWC Screw, Fixation, Bone 2 ALLY Bone Screw
5 00852776006522 PD-33-600 PD-33-600 The PMT Cervical Visualization Harness stretches to conform to the outer shoulde The PMT Cervical Visualization Harness stretches to conform to the outer shoulder while holding traction securely.It is used to achieve safe, effective traction on the shoulders for intraoperative cervical X-rays. HST Apparatus, Traction, Non-Powered 1 PMT Cervical Harness
6 00852776006515 PD-04-470 PD-04-470 CORUS Guide Tube Adapter LXH Orthopedic Manual Surgical Instrument 1 CORUS Guide Tube Adapter
7 00852776006188 DX-22-600 DX-22-600 A set of individual non-powered, disposable, hand-held surgical instruments inte A set of individual non-powered, disposable, hand-held surgical instruments intended and indicated for preparation of a spinal joint to aid in fusion. The set contains trial spacers, an awl, and a screwdriver. LXH Orthopedic Manual Surgical Instrument 1 DTRAX® Spinal System-L
8 10852776006024 PD-32-301 PD-32-301 The DTRAX Bone Screw is a single-use implant made of titanium alloy and used in The DTRAX Bone Screw is a single-use implant made of titanium alloy and used in bone reconstruction, osteotomy, arthrodesis, join fusion, fracture repair and fixation appropriate for the size of the device. HWC Screw, Fixation, Bone 2 DTRAX Bone Screw
9 00852776006430 DX-22-100 The CORUS Spinal System instruments are used to access and prepare the posterior The CORUS Spinal System instruments are used to access and prepare the posterior cervical spine for joint fusion by decortication of bone surfaces, including the posterior lateral mass and facet joints, combined with application of allograft or autograft in patients with or without anterior or posterior instrumentation. It is recommended that commercially available autograft or allograft be used to aid fusion. Autograft or allograft material is not supplied as part of the system. HRX Arthroscope CORUS™ Spinal System
10 00852776006362 PD-31-612 PD-31-612 CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heigh CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only. OVE Intervertebral Fusion Device With Integrated Fixation, Cervical 2 CAVUX™ Cervical Cage-L 9x14x17mm
11 00852776006355 PD-31-611 PD-31-611 CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heigh CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only. OVE Intervertebral Fusion Device With Integrated Fixation, Cervical 2 CAVUX™ Cervical Cage-L 8x14x17mm
12 00852776006348 PD-31-610 PD-31-610 CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heigh CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only. OVE Intervertebral Fusion Device With Integrated Fixation, Cervical 2 CAVUX™ Cervical Cage-L 7x14x17mm
13 00852776006300 PD-32-601 PD-32-601 The bone screw is indicated for use in bone reconstruction, osteotomy, arthrodes The bone screw is indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are intended for single use only. HWC Screw, Fixation, Bone 2 ALLY™ Bone Screw-L 10mm
14 00852776006287 PD-31-603 PD-31-603 CAVUX Cervical Cage is indicated for use in skeletally mature patients with dege CAVUX Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX™ Cervical Cage-L 9x12x15 mm 7 deg
15 00852776006508 DX-22-300 DX-22-300 HRX Arthroscope 2 CORUS Spinal System-X
16 00852776006089 DX-22-100 DX-22-100 The DTRAX® Spinal System is a set of instruments intended and indicated for acce The DTRAX® Spinal System is a set of instruments intended and indicated for access and preparation of a spinal joint to aid in fusion. HRX Arthroscope 2 DTRAX® Spinal System
17 00852776006492 PD-31-203 PD-31-203 ODP Intervertebral Fusion Device With Bone Graft, Cervical CAVUX Cervical Cage-X
18 20852776006069 PD-31-200 The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 DTRAX Cervical Cage-B
19 00852776006270 PD-31-602 PD-31-602 CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with de CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX™ Cervical Cage-L 8x12x15mm 7 deg
20 00852776006256 PD-31-600 PD-31-600 CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with de CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX™ Cervical Cage-L 6x12x15mm 7 deg
21 10852776006000 PD-31-200 PD-31-200 The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 DTRAX Cervical Cage-B
22 00852776006454 PD-10-400 A manual orthopedic surgical instrument used to deliver structural bone graft t A manual orthopedic surgical instrument used to deliver structural bone graft to a target area of the spine. The Allograft Delivery Instrument is manufactured using medical grade polycarbonate resin and stainless steel. The CORUS™ Allograft Delivery Instrument is intended and indicated for the delivery of structural bone graft to a target area of the spine. LXH Orthopedic Manual Surgical Instrument CORUS™ Allograft Delivery Instrument
23 00852776006423 PD-31-202 CAVUX® Cervical Cages are titanium constructs offered in various footprints and CAVUX® Cervical Cages are titanium constructs offered in various footprints and heights. All CAVUX® Cervical Cages are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are single-use only. ODP Intervertebral Fusion Device With Bone Graft, Cervical CAVUX™ Cervical Cage SB
24 00852776006263 PD-31-601 PD-31-601 CAVUX Cervical Cage is indicated for use in skeletally mature patients with dege CAVUX Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX™ Cervical Cage-L 7x12x15mm 7 deg
25 10852776006017 PD-31-100 PD-31-100 The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 DTRAX Cervical Cage-T
26 00852776006386 PD-31-220 CAVUX® Cervical Cages are titanium constructs offered in various footprints and CAVUX® Cervical Cages are titanium constructs offered in various footprints and heights. All CAVUX Cervical Cages are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are single-use only. ODP Intervertebral Fusion Device With Bone Graft, Cervical CAVUX™ Cervical Cage SE
27 00852776006331 PD-31-609 PD-31-609 CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heigh CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only. OVE Intervertebral Fusion Device With Integrated Fixation, Cervical CAVUX™ Cervical Cage-L 6x14x17mm
28 00852776006317 PD-32-602 PD-32-602 The bone screw is indicated for use in bone reconstruction, osteotomy, arthrodes The bone screw is indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. screws are intended for single use only. HWC Screw, Fixation, Bone 2 ALLY™ Bone Screw-L 12mm
29 00852776006003 PD-31-200 PD-31-200 The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant The DTRAX Cervical Cage-B is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX Cervical Cage-B
30 00852776006010 PD-31-100 PD-31-100 The CAVUX Cervical Cage-T is a single-use, titanium alloy intervertebral implant The CAVUX Cervical Cage-T is a single-use, titanium alloy intervertebral implant available in various footprints and heights. It is intended to be used in cervical spinal fusion surgery for skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 CAVUX Cervical Cage-T
Other products with the same Product Code "HWC"
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 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.
33 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.
34 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.
35 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.
36 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.
37 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.
38 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.
39 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.
40 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.
41 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.
42 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.
43 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.
44 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.
45 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.
46 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.
47 10381780123064 CSS500000670WT CSS500000670WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
48 10381780123057 CSS500000650WT CSS500000650WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
49 10381780123040 CSS500000640WT CSS500000640WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.
50 10381780123033 CSS500000630WT CSS500000630WT The washer is used in conjunction with the Capture High Torque Screw System. CAPTURE™ High Torque Screw System ASCENSION ORTHOPEDICS, INC.