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
8804-1205
In Commercial Distribution

  • 00888480569855 ()

  • ACF PEEK 0° 12X14X5MM
8804-1205

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0005
In Commercial Distribution

  • 00888480555308 ()

  • ACDF PEEK 0° 13X15X5MM
8411-0005

  • 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
8825-0750
In Commercial Distribution

  • 00887868212338 ()

  • VBR PEEK 7°/0° 14x18x50mm
8825-0750

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0747
In Commercial Distribution

  • 00887868212307 ()

  • VBR PEEK 7°/0° 14x18x47mm
8825-0747

  • 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
8825-0739
In Commercial Distribution

  • 00887868212222 ()

  • VBR PEEK 7°/0° 14x18x39mm
8825-0739

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0738
In Commercial Distribution

  • 00887868212215 ()

  • VBR PEEK 7°/0° 14x18x38mm
8825-0738

  • Polymeric spinal interbody fusion cage
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