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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Bone Graft Funnel
SEASPINE ORTHOPEDICS CORPORATION
SR-0377-01
In Commercial Distribution

  • 10889981171223 ()
SR-0377-01

  • Bone graft funnel
T-Handle Head Turner
SEASPINE ORTHOPEDICS CORPORATION
SR-0372
In Commercial Distribution

  • 10889981171148 ()
SR-0372

  • Orthopaedic implant inserter/extractor, reusable
Straight Impactor
SEASPINE ORTHOPEDICS CORPORATION
SR-0374
In Commercial Distribution

  • 10889981171131 ()
SR-0374

  • Orthopaedic implant impactor, reusable
T30 Inserter, Tapered
SEASPINE ORTHOPEDICS CORPORATION
SR-0375
In Commercial Distribution

  • 10889981171124 ()
SR-0375

  • Orthopaedic implant inserter/extractor, reusable
Bent Retractor, Right
SEASPINE ORTHOPEDICS CORPORATION
SR-0371
In Commercial Distribution

  • 10889981171117 ()
SR-0371

  • Hand-held surgical retractor, reusable
Bent Retractor, Left
SEASPINE ORTHOPEDICS CORPORATION
SR-0370
In Commercial Distribution

  • 10889981171100 ()
SR-0370

  • Hand-held surgical retractor, reusable
Bent Retractor
SEASPINE ORTHOPEDICS CORPORATION
SR-0358
In Commercial Distribution

  • 10889981171094 ()
SR-0358

  • Hand-held surgical retractor, reusable
Angled Cup Curette, Right
SEASPINE ORTHOPEDICS CORPORATION
SR-0334-RIGHT
In Commercial Distribution

  • 10889981171087 ()
SR-0334-RIGHT

  • Bone curette, reusable
Angled Cup Curette, Left
SEASPINE ORTHOPEDICS CORPORATION
SR-0334-LEFT
In Commercial Distribution

  • 10889981171070 ()
SR-0334-LEFT

  • Bone curette, reusable
Bayonetted Curette, Up Angled
SEASPINE ORTHOPEDICS CORPORATION
SR-0322-UP
In Commercial Distribution

  • 10889981171063 ()
SR-0322-UP

  • Bone curette, reusable
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