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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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LIF Trial, Rasped, 6 X 22 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-06227010
In Commercial Distribution

  • 00840180511596 ()


  • Spinal implant trial
LIF Trial, Rasped, 10 X 18 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-10187010
In Commercial Distribution

  • 00840180511572 ()


  • Spinal implant trial
LIF Trial, Rasped, 6 X 18 X 70, 10°, Hudson
ALPHATEC SPINE, INC.
CI-11084-10-06187010
In Commercial Distribution

  • 00840180511558 ()


  • Spinal implant trial
Cervical Trial, 4 x 16 x 14, 7°
ALPHATEC SPINE, INC.
CI-11010-10-04161407
In Commercial Distribution

  • 00840180509791 ()


  • Spinal implant trial
Cervical Trial, 3 x 14 x 12, 7°
ALPHATEC SPINE, INC.
CI-11010-10-03141207
In Commercial Distribution

  • 00840180509777 ()


  • Spinal implant trial
Cervical Trial Depth Marker, 18 MM
ALPHATEC SPINE, INC.
CI-10971-08181607
In Commercial Distribution

  • 00840180508480 ()


  • Spinal implant trial
Cervical Trial Depth Marker 16 MM
ALPHATEC SPINE, INC.
CI-10971-08161407
In Commercial Distribution

  • 00840180508473 ()


  • Spinal implant trial
Cervical Trial Depth Marker 14 mm
ALPHATEC SPINE, INC.
CI-10971-08141207
In Commercial Distribution

  • 00840180508466 ()


  • Spinal implant trial
U-Shaped Cervical Trial
ALPHATEC SPINE, INC.
CI-10972-10-10181607
In Commercial Distribution

  • 00840180508435 ()


  • Spinal implant trial
IdentiTi PC Trial, 6 x 10 x 25, 15-deg
ALPHATEC SPINE, INC.
CI-10864-06102515
In Commercial Distribution

  • 00840180506875 ()


  • Spinal implant trial
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