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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Interbody, 11mm x 24mm x 10mm, 5 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124104
In Commercial Distribution

  • 10889981189594 ()
TO1-124104

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 10mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124101
In Commercial Distribution

  • 10889981189587 ()
TO1-124101

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 9mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124095
In Commercial Distribution

  • 10889981189563 ()
TO1-124095

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 9mm, 5 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124094
In Commercial Distribution

  • 10889981189556 ()
TO1-124094

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 9mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124091
In Commercial Distribution

  • 10889981189549 ()
TO1-124091

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 8mm, 5 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124084
In Commercial Distribution

  • 10889981189525 ()
TO1-124084

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 8mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124081
In Commercial Distribution

  • 10889981189518 ()
TO1-124081

  • Vertebral body prosthesis
Interbody, 11mm x 24mm x 7mm, 5 Deg
SEASPINE ORTHOPEDICS CORPORATION
TO1-124074
In Commercial Distribution

  • 10889981189495 ()
TO1-124074

  • Vertebral body prosthesis
OsteoStrux® Strip, 15cc
SEASPINE ORTHOPEDICS CORPORATION
56010150ITL
In Commercial Distribution

  • 10889981123376 ()

  • 15cc
56010150ITL

  • Bone matrix implant, composite
OsteoStrux® Strip, 10cc
SEASPINE ORTHOPEDICS CORPORATION
56010100ITL
In Commercial Distribution

  • 10889981123369 ()

  • 10cc
56010100ITL

  • Bone matrix implant, composite
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