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 Class Implantable

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Trial, 35mm x 27mm x 10mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-111015
In Commercial Distribution

  • 10889981265601 ()
RA2-111015

  • Spinal implant trial
Trial, 31mm x 24mm x 20mm, 20 deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-102020
In Commercial Distribution

  • 10889981265588 ()
RA2-102020

  • 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
Trial, 31mm x 24mm x 16mm, 30 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101630
In Commercial Distribution

  • 10889981265526 ()
RA2-101630

  • Spinal implant trial
Trial, 31mm x 24mm x 14mm, 25 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101425
In Commercial Distribution

  • 10889981265502 ()
RA2-101425

  • Spinal implant trial
Trial, 35mm x 27mm x 10mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-101015
In Commercial Distribution

  • 10889981265489 ()
RA2-101015

  • Spinal implant trial
Spin Plate, 35mm x 27mm x 8mm
SEASPINE ORTHOPEDICS CORPORATION
RA1-352708
In Commercial Distribution

  • 10889981259525 ()
RA1-352708

  • Metal-polymer composite spinal interbody fusion cage
Trial Rasp, 43mm x 30mm x 14mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-241410
In Commercial Distribution

  • 10889981310059 ()
RA2-241410

  • Bone file/rasp, manual, reusable
Trial Rasp, 43mm x 30mm x 12mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-241215
In Commercial Distribution

  • 10889981310042 ()
RA2-241215

  • Bone file/rasp, manual, reusable
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