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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Trial, 18x15x12mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-12
In Commercial Distribution

  • 10889981178741 ()
SR-0419-12

  • Spinal implant trial
Trial, 18x15x11mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-11
In Commercial Distribution

  • 10889981178734 ()
SR-0419-11

  • Spinal implant trial
Trial, 18x15x10mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-10
In Commercial Distribution

  • 10889981178727 ()
SR-0419-10

  • Spinal implant trial
Trial, 18x15x9mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-09
In Commercial Distribution

  • 10889981178710 ()
SR-0419-09

  • Spinal implant trial
Trial, 18x15x8mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-08
In Commercial Distribution

  • 10889981178703 ()
SR-0419-08

  • Spinal implant trial
Trial, 18x15x7mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-07
In Commercial Distribution

  • 10889981178697 ()
SR-0419-07

  • Spinal implant trial
Trial, 18x15x6mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-06
In Commercial Distribution

  • 10889981178680 ()
SR-0419-06

  • Spinal implant trial
Trial, 18x15x5mm, 7 deg. Lordosis, w/o Stops
SEASPINE ORTHOPEDICS CORPORATION
SR-0419-05
In Commercial Distribution

  • 10889981178673 ()
SR-0419-05

  • Spinal implant trial
Cambria Trial, 15x13x12mm, Flat, Line to Line
SEASPINE ORTHOPEDICS CORPORATION
93-9942
In Commercial Distribution

  • 10889981055387 ()

  • 15x13x12mm
93-9942

  • Spinal implant trial
Cambria Trial, 15x13x11mm, Flat, Line to Line
SEASPINE ORTHOPEDICS CORPORATION
93-9941
In Commercial Distribution

  • 10889981055370 ()

  • 15x13x11mm
93-9941

  • Spinal implant trial
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