SEARCH RESULTS FOR: seaspine(25146 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, 35mm x 27mm x 16mm, 25 Deg
Seaspine Orthopedics Corporation
RA2-111625
In Commercial Distribution

  • 10889981265632 ()
RA2-111625

  • Spinal implant trial
Trial, 35mm x 27mm x 12mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-111220
In Commercial Distribution

  • 10889981265618 ()
RA2-111220

  • Spinal implant trial
Trial, 31mm x 24mm x 20mm, 30 deg
Seaspine Orthopedics Corporation
RA2-102030
In Commercial Distribution

  • 10889981265595 ()
RA2-102030

  • Spinal implant trial
Trial, 31mm x 24mm x 20mm, 15 deg
Seaspine Orthopedics Corporation
RA2-102015
In Commercial Distribution

  • 10889981265571 ()
RA2-102015

  • Spinal implant trial
Trial, 31mm x 24mm x 20mm, 10 deg
Seaspine Orthopedics Corporation
RA2-102010
In Commercial Distribution

  • 10889981265564 ()
RA2-102010

  • Spinal implant trial
Trial, 31mm x 24mm x 18mm, 15 Deg
Seaspine Orthopedics Corporation
RA2-101815
In Commercial Distribution

  • 10889981265540 ()
RA2-101815

  • Spinal implant trial
3-Hole No-Profile Interbody, 31mm x 24mm x 10mm, 10 Deg, 3D
Seaspine Orthopedics Corporation
WA1-301010
In Commercial Distribution

  • 10889981263676 ()
WA1-301010

  • Metallic spinal interbody fusion cage
Iliac Tap, 8.5mm
Seaspine Orthopedics Corporation
SR-0619-85
In Commercial Distribution

  • 10889981263652 ()
SR-0619-85

  • Bone tap, reusable
Safety Suction Tip #8
Seaspine Orthopedics Corporation
SR-0621
In Commercial Distribution

  • 10889981263560 ()
SR-0621

  • Surgical irrigation/aspiration cannula, non-illuminating, reusable
Distraction Forceps, Cervical
Seaspine Orthopedics Corporation
SR-0613
In Commercial Distribution

  • 10889981263553 ()
SR-0613

  • Bone distraction forceps
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