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
8825-0712
In Commercial Distribution

  • 00887868211959 ()

  • ACF PEEK 7°/0° 14x18x12mm
8825-0712

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0710
In Commercial Distribution

  • 00887868211935 ()

  • ACF PEEK 7°/0° 14x18x10mm
8825-0710

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0708
In Commercial Distribution

  • 00887868211911 ()

  • ACF PEEK 7°/0° 14x18x08mm
8825-0708

  • Polymeric spinal interbody fusion cage
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
8825-0747
In Commercial Distribution

  • 00887868212307 ()

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

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0745
In Commercial Distribution

  • 00887868212284 ()

  • VBR PEEK 7°/0° 14x18x45mm
8825-0745

  • 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
8825-0737
In Commercial Distribution

  • 00887868212208 ()

  • VBR PEEK 7°/0° 14x18x37mm
8825-0737

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0735
In Commercial Distribution

  • 00887868212185 ()

  • VBR PEEK 7°/0° 14x18x35mm
8825-0735

  • Polymeric spinal interbody fusion cage
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