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
OsteoBallast, 115 x11mm
SEASPINE ORTHOPEDICS CORPORATION
56800160
In Commercial Distribution

  • 10889981189266 ()
56800160

  • Bone matrix implant, human-derived
Ballast, 115 x11mm
SEASPINE ORTHOPEDICS CORPORATION
02-8000-160
In Commercial Distribution

  • 10889981189259 ()
02-8000-160

  • Bone matrix implant, human-derived
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