SEARCH RESULTS FOR: seaspine(6344 results)

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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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Plate Bender
SEASPINE ORTHOPEDICS CORPORATION
SR-0482
In Commercial Distribution

  • 10889981217297 ()
SR-0482

  • Manual orthopaedic bender, reusable
Trial, 39mm x 30mm x 20mm, 25 deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-132025
In Commercial Distribution

  • 10889981217105 ()
RA2-132025

  • Spinal implant trial
Trial, 39mm x 30mm x 18mm, 25 deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131825
In Commercial Distribution

  • 10889981217099 ()
RA2-131825

  • Spinal implant trial
Trial, 39mm x 30mm x 18mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131820
In Commercial Distribution

  • 10889981217082 ()
RA2-131820

  • Spinal implant trial
Trial, 39mm x 30mm x 16mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131620
In Commercial Distribution

  • 10889981217075 ()
RA2-131620

  • Spinal implant trial
Trial, 39mm x 30mm x 16mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131615
In Commercial Distribution

  • 10889981217068 ()
RA2-131615

  • Spinal implant trial
Trial, 39mm x 30mm x 16mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131610
In Commercial Distribution

  • 10889981217051 ()
RA2-131610

  • Spinal implant trial
Trial, 39mm x 30mm x 14mm, 20 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131420
In Commercial Distribution

  • 10889981217044 ()
RA2-131420

  • Spinal implant trial
Trial, 39mm x 30mm x 14mm, 15 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131415
In Commercial Distribution

  • 10889981217037 ()
RA2-131415

  • Spinal implant trial
Trial, 39mm x 30mm x 14mm, 10 Deg
SEASPINE ORTHOPEDICS CORPORATION
RA2-131410
In Commercial Distribution

  • 10889981217020 ()
RA2-131410

  • Spinal implant trial
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