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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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TRIAL RASP, STRAIGHT, 19MM WIDE, 6MM
SPINEFRONTIER, INC.
11-50249-06
In Commercial Distribution

  • 00190361038382 ()


  • Polymeric spinal interbody fusion cage
TRIAL, LORDOTIC, 19MM WIDE, 16MM
SPINEFRONTIER, INC.
11-50121-16
In Commercial Distribution

  • 00190361038375 ()


  • Polymeric spinal interbody fusion cage
TRIAL, LORDOTIC, 19MM WIDE, 14MM
SPINEFRONTIER, INC.
11-50121-14
In Commercial Distribution

  • 00190361038368 ()


  • Polymeric spinal interbody fusion cage
TRIAL, LORDOTIC, 19MM WIDE, 10MM
SPINEFRONTIER, INC.
11-50121-10
In Commercial Distribution

  • 00190361038344 ()


  • Polymeric spinal interbody fusion cage
TRIAL, LORDOTIC, 19MM WIDE, 8MM
SPINEFRONTIER, INC.
11-50121-08
In Commercial Distribution

  • 00190361038337 ()


  • Polymeric spinal interbody fusion cage
TRIAL STRAIGHT, 14MM X 19MM
SPINEFRONTIER, INC.
11-50108-14
In Commercial Distribution

  • 00190361038313 ()


  • Polymeric spinal interbody fusion cage
TRIAL, STRAIGHT, 19MM WIDE, 10MM
SPINEFRONTIER, INC.
11-50251-10
In Commercial Distribution

  • 00190361038269 ()


  • Polymeric spinal interbody fusion cage
TRIAL, STRAIGHT, 19MM WIDE, 8MM
SPINEFRONTIER, INC.
11-50251-08
In Commercial Distribution

  • 00190361038245 ()


  • Polymeric spinal interbody fusion cage
TRIAL, STRAIGHT, 19MM WIDE, 4MM
SPINEFRONTIER, INC.
11-50251-04
In Commercial Distribution

  • 00190361038221 ()


  • Polymeric spinal interbody fusion cage
TRIAL RASP, ANGLED, 22MM WIDE, 6MM
SPINEFRONTIER, INC.
11-50062-06
In Commercial Distribution

  • 00190361038177 ()


  • Polymeric spinal interbody fusion cage
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