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 30mm x 12mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-131220
In Commercial Distribution

  • 10889981265854 ()
RA2-131220

  • Spinal implant trial
Trial, 39mm x 27mm x 20mm, 20 deg
Seaspine Orthopedics Corporation
RA2-122020
In Commercial Distribution

  • 10889981265823 ()
RA2-122020

  • 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, 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 12mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-111220
In Commercial Distribution

  • 10889981265618 ()
RA2-111220

  • Spinal implant trial
Trial, 31mm x 24mm x 20mm, 20 deg
Seaspine Orthopedics Corporation
RA2-102020
In Commercial Distribution

  • 10889981265588 ()
RA2-102020

  • Spinal implant trial
Trial, 31mm x 24mm x 12mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-101220
In Commercial Distribution

  • 10889981265496 ()
RA2-101220

  • Spinal implant trial
Trial, 39mm x 30mm x 18mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-131820
In Commercial Distribution

  • 10889981217082 ()
RA2-131820

  • Spinal implant trial
Trial, 39mm x 30mm x 16mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-131620
In Commercial Distribution

  • 10889981217075 ()
RA2-131620

  • Spinal implant trial
Trial, 39mm x 30mm x 14mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-131420
In Commercial Distribution

  • 10889981217044 ()
RA2-131420

  • Spinal implant trial
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