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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Kerrison-40 Deg Up Bite 5mm
SEASPINE ORTHOPEDICS CORPORATION
06-50-0143
In Commercial Distribution

  • 10889981104351 ()

  • 40 Deg, 5mm
06-50-0143

  • Spinal rongeur
Kerrison-40 Deg Up Bite 4mm
SEASPINE ORTHOPEDICS CORPORATION
06-50-0142
In Commercial Distribution

  • 10889981104344 ()

  • 40 Deg, 4mm
06-50-0142

  • Spinal rongeur
Kerrison-40 Deg Up Bite 3mm
SEASPINE ORTHOPEDICS CORPORATION
06-50-0141
In Commercial Distribution

  • 10889981104337 ()

  • 40 Deg, 3mm
06-50-0141

  • Spinal rongeur
Kerrison-40 Deg Up Bite 2mm
SEASPINE ORTHOPEDICS CORPORATION
06-50-0140
In Commercial Distribution

  • 10889981104320 ()

  • 40 Deg, 2mm
06-50-0140

  • Spinal rongeur
Cup-#3 Pull Rev Bayonetted
SEASPINE ORTHOPEDICS CORPORATION
06-50-0114
In Commercial Distribution

  • 10889981104238 ()
06-50-0114

  • Bone curette, reusable
Cup-#3 Pull Fwd Bayonetted
SEASPINE ORTHOPEDICS CORPORATION
06-50-0113
In Commercial Distribution

  • 10889981104221 ()
06-50-0113

  • Bone curette, reusable
Cup-#3 Left 30 Deg Bayonetted
SEASPINE ORTHOPEDICS CORPORATION
06-50-0112
In Commercial Distribution

  • 10889981104214 ()

  • 30 Deg
06-50-0112

  • Bone curette, reusable
Cup-#3 Right 30 Deg Bayonetted
SEASPINE ORTHOPEDICS CORPORATION
06-50-0111
In Commercial Distribution

  • 10889981104207 ()

  • 30 Deg
06-50-0111

  • Bone curette, reusable
Cup-#3 Fwd Bayonetted
SEASPINE ORTHOPEDICS CORPORATION
06-50-0110
In Commercial Distribution

  • 10889981104191 ()
06-50-0110

  • Bone curette, reusable
Cup-#0 Pull Rev Bayonetted
SEASPINE ORTHOPEDICS CORPORATION
06-50-0092
In Commercial Distribution

  • 10889981104139 ()
06-50-0092

  • Bone curette, reusable
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