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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No Description
BIOMET SPINE LLC
8880-0110
In Commercial Distribution

  • 00888480572541 ()

  • ALIF PEEK 0° 24X32X10MM
8880-0110

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0108
In Commercial Distribution

  • 00888480572534 ()

  • ALIF PEEK 0° 24X32X8MM
8880-0108

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
07.01707.022
In Commercial Distribution

  • 00889024328013 ()

  • Polyaxial Smooth Shank Screw Ø4.0 mm X 24 mm L
07.01707.022

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8825-0749
In Commercial Distribution

  • 00887868212321 ()

  • VBR PEEK 7°/0° 14x18x49mm
8825-0749

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0748
In Commercial Distribution

  • 00887868212314 ()

  • VBR PEEK 7°/0° 14x18x48mm
8825-0748

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0746
In Commercial Distribution

  • 00887868212291 ()

  • VBR PEEK 7°/0° 14x18x46mm
8825-0746

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0744
In Commercial Distribution

  • 00887868212277 ()

  • VBR PEEK 7°/0° 14x18x44mm
8825-0744

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0742
In Commercial Distribution

  • 00887868212253 ()

  • VBR PEEK 7°/0° 14x18x42mm
8825-0742

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0741
In Commercial Distribution

  • 00887868212246 ()

  • VBR PEEK 7°/0° 14x18x41mm
8825-0741

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0740
In Commercial Distribution

  • 00887868212239 ()

  • VBR PEEK 7°/0° 14x18x40mm
8825-0740

  • Polymeric spinal interbody fusion cage
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