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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DILATOR 2
SEASPINE ORTHOPEDICS CORPORATION
MM2-000140
In Commercial Distribution

  • 10889981178154 ()
MM2-000140

  • Orthopaedic prosthesis implantation positioning instrument, reusable
DILATOR 1, 1/4 SQUARE
SEASPINE ORTHOPEDICS CORPORATION
MM2-000130
In Commercial Distribution

  • 10889981178147 ()
MM2-000130

  • Orthopaedic prosthesis implantation positioning instrument, reusable
DILATOR 1
SEASPINE ORTHOPEDICS CORPORATION
MM2-000110
In Commercial Distribution

  • 10889981178130 ()
MM2-000110

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Modular Trial, 14 x 13 x 12mm, 10 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2112
In Commercial Distribution

  • 10889981177447 ()
86-2112

  • Spinal implant trial
Modular Trial, 14 x 13 x 10mm, 10 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2110
In Commercial Distribution

  • 10889981177423 ()
86-2110

  • Spinal implant trial
Modular Trial, 14 x 13 x 9mm, 10 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2109
In Commercial Distribution

  • 10889981177416 ()
86-2109

  • Spinal implant trial
Modular Trial, 14 x 13 x 8mm, 10 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2108
In Commercial Distribution

  • 10889981177409 ()
86-2108

  • Spinal implant trial
Modular Trial, 14 x 13 x 6mm, 10 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2106
In Commercial Distribution

  • 10889981177386 ()
86-2106

  • Spinal implant trial
Modular Trial, 20 x 15 x 11mm, 7 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2011
In Commercial Distribution

  • 10889981177362 ()
86-2011

  • Spinal implant trial
Modular Trial, 20 x 15 x 10mm, 7 Deg Lordosis
SEASPINE ORTHOPEDICS CORPORATION
86-2010
In Commercial Distribution

  • 10889981177355 ()
86-2010

  • Spinal implant trial
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