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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 Device Size Type Device Class Implantable

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Trial, 39mm x 27mm x 16mm, 30 Deg
Seaspine Orthopedics Corporation
RA2-121630
In Commercial Distribution

  • 10889981265762 ()
RA2-121630

  • Spinal implant trial
Trial, 39mm x 27mm x 16mm, 25 Deg
Seaspine Orthopedics Corporation
RA2-121625
In Commercial Distribution

  • 10889981265755 ()
RA2-121625

  • Spinal implant trial
Trial, 39mm x 27mm x 14mm, 25 Deg
Seaspine Orthopedics Corporation
RA2-121425
In Commercial Distribution

  • 10889981265748 ()
RA2-121425

  • Spinal implant trial
Trial, 39mm x 27mm x 12mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-121220
In Commercial Distribution

  • 10889981265731 ()
RA2-121220

  • Spinal implant trial
Trial, 39mm x 27mm x 10mm, 15 Deg
Seaspine Orthopedics Corporation
RA2-121015
In Commercial Distribution

  • 10889981265724 ()
RA2-121015

  • Spinal implant trial
Trial, 35mm x 27mm x 20mm, 30 deg
Seaspine Orthopedics Corporation
RA2-112030
In Commercial Distribution

  • 10889981265717 ()
RA2-112030

  • Spinal implant trial
Trial, 35mm x 27mm x 20mm, 20 deg
Seaspine Orthopedics Corporation
RA2-112020
In Commercial Distribution

  • 10889981265700 ()
RA2-112020

  • Spinal implant trial
Trial, 35mm x 27mm x 20mm, 15 deg
Seaspine Orthopedics Corporation
RA2-112015
In Commercial Distribution

  • 10889981265694 ()
RA2-112015

  • Spinal implant trial
Trial, 35mm x 27mm x 20mm, 10 deg
Seaspine Orthopedics Corporation
RA2-112010
In Commercial Distribution

  • 10889981265687 ()
RA2-112010

  • Spinal implant trial
Trial, 35mm x 27mm x 18mm, 30 deg
Seaspine Orthopedics Corporation
RA2-111830
In Commercial Distribution

  • 10889981265670 ()
RA2-111830

  • Spinal implant trial
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