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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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90mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-090
In Commercial Distribution

  • 00190376316574 ()


  • Surgical retraction system, reusable
80mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-080
In Commercial Distribution

  • 00190376316567 ()


  • Surgical retraction system, reusable
70mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-070
In Commercial Distribution

  • 00190376316550 ()


  • Surgical retraction system, reusable
60mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-060
In Commercial Distribution

  • 00190376316543 ()


  • Surgical retraction system, reusable
50mm C-C Blade, Sigma TLIF
ALPHATEC SPINE, INC.
269-150-050
In Commercial Distribution

  • 00190376316536 ()


  • Surgical retraction system, reusable
ROD B02223645 D-ROD CC 6X450MM
MEDICREA INTERNATIONAL
B02223645
In Commercial Distribution

  • 03613720294597 ()


  • Bone-screw internal spinal fixation system rod
LIF, RASP, CC OFFSET, 22MM
ALPHATEC SPINE, INC.
256-16-100-22
In Commercial Distribution

  • 00190376394411 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 20MM
ALPHATEC SPINE, INC.
256-16-100-20
In Commercial Distribution

  • 00190376394404 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 18MM
ALPHATEC SPINE, INC.
256-16-100-18
In Commercial Distribution

  • 00190376394398 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 16MM
ALPHATEC SPINE, INC.
256-16-100-16
In Commercial Distribution

  • 00190376394381 ()


  • Bone file/rasp, manual, reusable
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