SEARCH RESULTS FOR: seaspine(201 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Type Device Class Implantable

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Integra Expandable Interbody - 10889981049461

8mm Trial (22x10mm, 0 deg). The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2108
Not in Commercial Distribution

  • 10889981049461 ()

  • 8mm (22x10mm, 0°)
98-2108

  • Orthopaedic implant inserter/extractor, reusable

Integra Expandable Interbody - 10889981049454

6mm Starter Trial. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2105
Not in Commercial Distribution

  • 10889981049454 ()

  • 6mm
98-2105

  • Orthopaedic implant inserter/extractor, reusable

Integra Expandable Interbody - 10889981049447

12mm Wide Removal Tool. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2012
Not in Commercial Distribution

  • 10889981049447 ()

  • 12mm
98-2012

  • Orthopaedic implant inserter/extractor, reusable

Integra Expandable Interbody - 10889981049430

Removal Tool. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2011
Not in Commercial Distribution

  • 10889981049430 ()
98-2011

  • Orthopaedic implant inserter/extractor, reusable

Integra Expandable Interbody - 10889981049423

Expansion Driver. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2010
Not in Commercial Distribution

  • 10889981049423 ()

  • 10mm
98-2010

  • Orthopaedic implant inserter/extractor, reusable

Integra Expandable Interbody - 10889981049409

Inserter. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2001
Not in Commercial Distribution

  • 10889981049409 ()
98-2001

  • Orthopaedic implant inserter/extractor, reusable

Integra Expandable Interbody - 10889981049393

Inserter. The Integra Expandable IBD System consists of lumbar interbody fusion devices manufactured from PEEK-OPTIMA® LT1 (ASYM F2026), titanium (Ti-6AI-4V ELI per ASTM F136) and cobalt chromium (Co-28Cr-6Mo per ASTM F1537) materials, with radiopaque tantalum markers (ASTM F560). These implants are generally box shaped with surface teeth and a central channel to be filled with autogenous bone graft.
SEASPINE ORTHOPEDICS CORPORATION
98-2000
Not in Commercial Distribution

  • 10889981049393 ()
98-2000

  • Orthopaedic implant inserter/extractor, reusable

Vu ePOD™ - 10889981049003

26mm Trial, 10 Deg, 16 mm
SEASPINE ORTHOPEDICS CORPORATION
14-26-2616
In Commercial Distribution

  • 10889981049003 ()

  • 26mm , 10°, 16 mm
14-26-2616

  • Orthopaedic implant inserter/extractor, reusable

Vu ePOD™ - 10889981048990

26mm Trial, 10 Deg, 15 mm
SEASPINE ORTHOPEDICS CORPORATION
14-26-2615
In Commercial Distribution

  • 10889981048990 ()

  • 26mm , 10°, 15 mm
14-26-2615

  • Orthopaedic implant inserter/extractor, reusable

Vu ePOD™ - 10889981048983

26mm Trial, 10 Deg, 14 mm
SEASPINE ORTHOPEDICS CORPORATION
14-26-2614
In Commercial Distribution

  • 10889981048983 ()

  • 26mm , 10°, 14 mm
14-26-2614

  • Orthopaedic implant inserter/extractor, reusable
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