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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Paddle Scraper, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3478
In Commercial Distribution

  • 10889981088804 ()

  • 8mm
93-3478

  • Bone file
Paddle Distractor, Long, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3461
In Commercial Distribution

  • 10889981088682 ()

  • 8mm
93-3461

  • Orthopaedic surgical distractor, internal
Paddle Distractor, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3446
In Commercial Distribution

  • 10889981088569 ()

  • 8mm
93-3446

  • Orthopaedic surgical distractor, internal
Bullet Distractor, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3416
In Commercial Distribution

  • 10889981088453 ()

  • 8mm
93-3416

  • Orthopaedic surgical distractor, internal
Paddle Scraper, Long, Convex, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3691
In Commercial Distribution

  • 10889981089474 ()

  • 8mm
93-3691

  • Bone file
Long Bullet Distractor, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3616
In Commercial Distribution

  • 10889981089351 ()

  • 8mm
93-3616

  • Orthopaedic surgical distractor, internal
Paddle Scraper, Convex, 8mm
SEASPINE ORTHOPEDICS CORPORATION
93-3601
In Commercial Distribution

  • 10889981089238 ()

  • 8mm
93-3601

  • Bone file
8mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4178
In Commercial Distribution

  • 10889981058326 ()

  • 8mm
93-4178

  • Spinal implant trial
8mm Hollywood Trial, Lordotic, Short
SEASPINE ORTHOPEDICS CORPORATION
93-4232
In Commercial Distribution

  • 10889981031084 ()

  • 8mm
93-4232

  • Spinal implant trial
8mm Long Ventura Trial
SEASPINE ORTHOPEDICS CORPORATION
93-3376
In Commercial Distribution

  • 10889981033316 ()

  • 8mm
93-3376

  • Spinal implant trial
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