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, 1/3 Rasped, Grooves, 4 x 18 x 70 x 10°
ALPHATEC SPINE, INC.
CI-11070-10-04187010
In Commercial Distribution

  • 00840180511176 ()


  • Spinal implant trial
Cranial Angled Trial Inserter, 15°
ALPHATEC SPINE, INC.
CI-11028
In Commercial Distribution

  • 00840180510711 ()


  • Orthopaedic implant inserter/extractor, reusable
Inserter/Distractor, Squid, Enlarged Slot
ALPHATEC SPINE, INC.
CI-10982
In Commercial Distribution

  • 00840180510438 ()


  • Orthopaedic implant inserter/extractor, reusable
ALIF Trial Rasp Template, 4 x 38 x 28mm
ALPHATEC SPINE, INC.
CI-11003-043828
In Commercial Distribution

  • 00840180510339 ()


  • Spinal implant trial
ALIF Trial Rasp Template, 4 x 34 x 24mm
ALPHATEC SPINE, INC.
CI-11003-043424
In Commercial Distribution

  • 00840180510322 ()


  • Spinal implant trial
LTX SPACER, 6 x 22 x 55 mm, 15°
ALPHATEC SPINE, INC.
261-06225515
In Commercial Distribution

  • 00190376522890 ()


  • Polymeric spinal interbody fusion cage
LTX DOMED SPACER, 6 x 22 x 50 mm, 20°
ALPHATEC SPINE, INC.
261-06225020-D
In Commercial Distribution

  • 00190376522883 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 22 x 50 mm, 20°
ALPHATEC SPINE, INC.
261-06225020
In Commercial Distribution

  • 00190376522876 ()


  • Polymeric spinal interbody fusion cage
LTX DOMED SPACER, 6 x 22 x 50 mm, 15°
ALPHATEC SPINE, INC.
261-06225015-D
In Commercial Distribution

  • 00190376522869 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 22 x 50 mm, 15°
ALPHATEC SPINE, INC.
261-06225015
In Commercial Distribution

  • 00190376522852 ()


  • Polymeric spinal interbody fusion cage
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