SEARCH RESULTS FOR: seaspine(22323 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 Device Size Type Device Class Implantable

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Trial, 31mm x 24mm x 18mm, 30 deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101830
In Commercial Distribution

  • 10889981265557 ()
RA2-101830

  • Spinal implant trial
Trial, 31mm x 24mm x 16mm, 30 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101630
In Commercial Distribution

  • 10889981265526 ()
RA2-101630

  • Spinal implant trial
Trial, 31mm x 24mm x 16mm, 25 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101625
In Commercial Distribution

  • 10889981265519 ()
RA2-101625

  • Spinal implant trial
Trial, 31mm x 24mm x 12mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101220
In Commercial Distribution

  • 10889981265496 ()
RA2-101220

  • Spinal implant trial
25° Medial/Lateral Angled Rake Curette
SEASPINE ORTHOPEDICS CORPORATION
SR-0607
In Commercial Distribution

  • 10889981265465 ()
SR-0607

  • Bone curette, reusable
25° Angled Lateral Cobb, 18mm, M/L Right
SEASPINE ORTHOPEDICS CORPORATION
SR-0605
In Commercial Distribution

  • 10889981265441 ()
SR-0605

  • Bone lever/elevator, reusable
Iliac Tap, 6.5mm
SEASPINE ORTHOPEDICS CORPORATION
SR-0619-65
In Commercial Distribution

  • 10889981263669 ()
SR-0619-65

  • Bone tap, reusable
Iliac Tap, 7.5mm
SEASPINE ORTHOPEDICS CORPORATION
SR-0619-75
In Commercial Distribution

  • 10889981263645 ()
SR-0619-75

  • Bone tap, reusable
Distraction Forceps, Cervical
SEASPINE ORTHOPEDICS CORPORATION
SR-0613
In Commercial Distribution

  • 10889981263553 ()
SR-0613

  • Bone distraction forceps
Osteophyte Remover
SEASPINE ORTHOPEDICS CORPORATION
SR-0590
In Commercial Distribution

  • 10889981263478 ()
SR-0590

  • Bone file/rasp, manual, reusable
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