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 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
5 00852776006515 PD-04-470 PD-04-470 CORUS Guide Tube Adapter LXH Orthopedic Manual Surgical Instrument 1 CORUS Guide Tube Adapter
6 20852776006021 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
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 18257200119226 11-1109-6 9mm x 50 mm SambaScrew SambaScrew ORTHOFIX INC.
2 18257200119219 11-1109-5 9mm x 45 mm SambaScrew SambaScrew ORTHOFIX INC.
3 18257200119202 11-1109-4 9mm x 40 mm SambaScrew SambaScrew ORTHOFIX INC.
4 18257200119196 11-1109-3 9mm x 35mm SambaScrew SambaScrew ORTHOFIX INC.
5 18257200119189 11-1109-2 9mm x 30mm SambaScrew SambaScrew ORTHOFIX INC.
6 18257200119172 11-1109-1 9mm x 25mm SambaScrew SambaScrew ORTHOFIX INC.
7 18056099649605 1 450502C TL PLUS FOOT&ANKLE KIT TRAY COMPLETE TRUELOK SYSTEM ORTHOFIX SRL
8 18056099649391 1 54-1214 TL PLUS X-WIRE WITHOUT OLIVE L300MM D1.5MM TRUELOK SYSTEM ORTHOFIX SRL
9 18056099649384 1 54-1213 TL PLUS X-WIRE WITH OLIVE L300MM D1.5MM TRUELOK SYSTEM ORTHOFIX SRL
10 18056099649377 1 54-1218 TL PLUS BAYONET WIRE WITHOUT OLIVE L300MM D1.5MM TRUELOK SYSTEM ORTHOFIX SRL
11 18056099649360 1 54-1217 TL PLUS BAYONET WIRE WITH OLIVE L300MM D1.5MM TRUELOK SYSTEM ORTHOFIX SRL
12 18056099647847 1 003-E-00001R L-PLATE, RIGHT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
13 18056099647830 1 003-E-00001L L-PLATE, LEFT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
14 18056099647823 1 003-D-03001 STRAIGHT PLATE, 6 HOLE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
15 18056099647816 1 003-D-02001 STRAIGHT PLATE, 4 HOLE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
16 18056099647809 1 003-D-01001 STRAIGHT PLATE, 3 HOLE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
17 18056099647793 1 003-C-02001 Y-PLATE, LARGE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
18 18056099647786 1 003-C-01001 Y-PLATE, SMALL VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
19 18056099647779 1 003-B-02001 T-PLATE, LARGE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
20 18056099647762 1 003-B-01001 T-PLATE, SMALL VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
21 18056099647755 1 002-H-00012 EVANS PLATE, 12MM SPACER VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
22 18056099647748 1 002-H-00010 EVANS PLATE, 10MM SPACER VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
23 18056099647731 1 002-H-00008 EVANS PLATE, 8MM SPACER VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
24 18056099647724 1 002-H-00006 EVANS PLATE, 6MM SPACER VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
25 18056099647717 1 002-G-01030 CC PLATE, LARGE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
26 18056099647700 1 002-G-01025 CC PLATE, MEDIUM VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
27 18056099647694 1 002-G-01020 CC PLATE, SMALL VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
28 18056099647687 1 002-F-01030 TN PLATE, LARGE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
29 18056099647670 1 002-F-01025 TN PLATE, MEDIUM VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
30 18056099647663 1 002-F-01020 TN PLATE, SMALL VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
31 18056099647656 1 002-C-02002R LAPIDUS PLATE, LARGE, 2MM STEP, RIGHT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
32 18056099647649 1 002-C-02002L LAPIDUS PLATE, LARGE, 2MM STEP, LEFT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
33 18056099647632 1 002-C-02000R LAPIDUS PLATE, LARGE, 0MM STEP, RIGHT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
34 18056099647625 1 002-C-02000L LAPIDUS PLATE, LARGE, 0MM STEP, LEFT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
35 18056099647618 1 002-C-01002R LAPIDUS PLATE, SMALL, 2MM STEP, RIGHT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
36 18056099647601 1 002-C-01002L LAPIDUS PLATE, SMALL, 2MM STEP, LEFT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
37 18056099647595 1 002-C-01000R LAPIDUS PLATE, SMALL, 0MM STEP, RIGHT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
38 18056099647588 1 002-C-01000L LAPIDUS PLATE, SMALL, 0MM STEP, LEFT VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
39 18056099647571 1 002-B-03003 MTP PLATE, LARGE VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
40 18056099647564 1 002-B-02002 MTP PLATE, MEDIUM VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
41 18056099647557 1 002-B-01001 MTP PLATE, SMALL VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
42 18056099647519 1 002-A-00003 OLIVE WIRES VIEW PLATING SYSTEM, REDUCE FRACTURE PLATING SYSTEM ORTHOFIX SRL
43 18056099647397 1 000-K-007C RIVAL BITE HEADLESS SCREW LARGE KIT D 7.5MM, D 7.5TMM BITE COMPRESSION SCREWS ORTHOFIX SRL
44 18056099647380 1 000-K-006C RIVAL BITE HEADLESS SCREW LARGE KIT D 6.5MM, D 6.5TMM BITE COMPRESSION SCREWS ORTHOFIX SRL
45 18056099647373 1 000-K-005C RIVAL BITE HEADLESS SCREW SMALL KIT D 2.5MM, D 3.0MM, D 4.0MM BITE COMPRESSION SCREWS ORTHOFIX SRL
46 18056099647366 1 000-K-004C RIVAL BITE LOW PROFILE HEADED SCREW LARGE KIT D 8.0MM, D 8.0TMM BITE COMPRESSION SCREWS ORTHOFIX SRL
47 18056099647359 1 000-K-003C RIVAL BITE LOW PROFILE HEADED SCREW LARGE KIT D 6.5MM, D 6.5TMM BITE COMPRESSION SCREWS ORTHOFIX SRL
48 18056099647342 1 000-K-002C RIVAL BITE LOW PROFILE HEADED SCREW MEDIUM KIT D 3.5MM, D 4.0MM BITE COMPRESSION SCREWS ORTHOFIX SRL
49 18056099647335 1 000-K-001C RIVAL BITE LOW PROFILE HEADED SCREW SMALL KIT D 2.0MM, D 2.5MM, D 3.0MM BITE COMPRESSION SCREWS ORTHOFIX SRL
50 18056099647328 1 001-A-65011 CANNULATED HEX DRIVER, 6.5/7.5MM HEADLESS SCREW, QUICK CONNECT BITE COMPRESSION SCREWS ORTHOFIX SRL