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
1400-0002
In Commercial Distribution

  • 00888480185246 ()

  • SOLITAIRE NARROW 12MM / 0°
1400-0002

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
1400-0000
In Commercial Distribution

  • 00888480185239 ()

  • SOLITAIRE NARROW 10MM / 0°
1400-0000

  • Vertebral body prosthesis
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
8825-0748
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
8825-0743
In Commercial Distribution

  • 00887868212260 ()

  • VBR PEEK 7°/0° 14x18x43mm
8825-0743

  • 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
8825-0740
In Commercial Distribution

  • 00887868212239 ()

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

  • Polymeric spinal interbody fusion cage
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