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, Long, Convex, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3699
In Commercial Distribution

  • 10889981089559 ()

  • 16mm
93-3699

  • Bone file
Long Bullet Distractor, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3624
In Commercial Distribution

  • 10889981089436 ()

  • 16mm
93-3624

  • Orthopaedic surgical distractor, internal
Paddle Scraper, Convex, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3609
In Commercial Distribution

  • 10889981089313 ()

  • 16mm
93-3609

  • Bone file
Paddle Scraper, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3486
In Commercial Distribution

  • 10889981088880 ()

  • 16mm
93-3486

  • Bone file
Paddle Distractor, Long, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3469
In Commercial Distribution

  • 10889981088767 ()

  • 16mm
93-3469

  • Orthopaedic surgical distractor, internal
Paddle Distractor, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3454
In Commercial Distribution

  • 10889981088644 ()

  • 16mm
93-3454

  • Orthopaedic surgical distractor, internal
Bullet Distractor, 16mm
SEASPINE ORTHOPEDICS CORPORATION
93-3424
In Commercial Distribution

  • 10889981088538 ()

  • 16mm
93-3424

  • Orthopaedic surgical distractor, internal
16mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4186
In Commercial Distribution

  • 10889981058401 ()

  • 16mm
93-4186

  • Spinal implant trial
16mm Long Ventura Trial
SEASPINE ORTHOPEDICS CORPORATION
93-3384
In Commercial Distribution

  • 10889981033392 ()

  • 16mm
93-3384

  • Spinal implant trial
16mm Hollywood Trial, Lordotic
SEASPINE ORTHOPEDICS CORPORATION
93-4259
In Commercial Distribution

  • 10889981031282 ()

  • 16mm
93-4259

  • Spinal implant trial
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