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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Trial Drill Guide, 9mm
SEASPINE ORTHOPEDICS CORPORATION
AP2-000409
In Commercial Distribution

  • 10889981239404 ()
AP2-000409

  • Spinal implant trial
Trial Drill Guide, 8mm
SEASPINE ORTHOPEDICS CORPORATION
AP2-000408
In Commercial Distribution

  • 10889981239398 ()
AP2-000408

  • Spinal implant trial
Trial Drill Guide, 7mm
SEASPINE ORTHOPEDICS CORPORATION
AP2-000407
In Commercial Distribution

  • 10889981239381 ()
AP2-000407

  • Spinal implant trial
Trial Drill Guide, 6mm
SEASPINE ORTHOPEDICS CORPORATION
AP2-000406
In Commercial Distribution

  • 10889981239374 ()
AP2-000406

  • Spinal implant trial
Trial Drill Guide, 5mm
SEASPINE ORTHOPEDICS CORPORATION
AP2-000405
In Commercial Distribution

  • 10889981239367 ()
AP2-000405

  • Spinal implant trial
Trial Drill Guide Inserter
SEASPINE ORTHOPEDICS CORPORATION
AP2-000401
In Commercial Distribution

  • 10889981239350 ()
AP2-000401

  • Spinal implant trial
Trial, 43mm x 30mm x 10mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-141010
In Commercial Distribution

  • 10889981265953 ()
RA2-141010

  • Spinal implant trial
Trial, 43mm x 30mm x 8mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-140810
In Commercial Distribution

  • 10889981265946 ()
RA2-140810

  • Spinal implant trial
Trial, 39mm x 30mm x 20mm, 30 deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-132030
In Commercial Distribution

  • 10889981265939 ()
RA2-132030

  • Spinal implant trial
Trial, 39mm x 30mm x 20mm, 20 deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-132020
In Commercial Distribution

  • 10889981265922 ()
RA2-132020

  • Spinal implant trial
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