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
8825-0719
In Commercial Distribution

  • 00887868212024 ()

  • VBR PEEK 7°/0° 14x18x19mm
8825-0719

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0717
In Commercial Distribution

  • 00887868212000 ()

  • VBR PEEK 7°/0° 14x18x17mm
8825-0717

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0715
In Commercial Distribution

  • 00887868211980 ()

  • VBR PEEK 7°/0° 14x18x15mm
8825-0715

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0713
In Commercial Distribution

  • 00887868211966 ()

  • VBR PEEK 7°/0° 14x18x13mm
8825-0713

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0711
In Commercial Distribution

  • 00887868211942 ()

  • ACF PEEK 7°/0° 14x18x11mm
8825-0711

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0709
In Commercial Distribution

  • 00887868211928 ()

  • ACF PEEK 7°/0° 14x18x09mm
8825-0709

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0707
In Commercial Distribution

  • 00887868211904 ()

  • ACF PEEK 7°/0° 14x18x07mm
8825-0707

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0706
In Commercial Distribution

  • 00887868211898 ()

  • ACF PEEK 7°/0° 14x18x06mm
8825-0706

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0705
In Commercial Distribution

  • 00887868211881 ()

  • ACF PEEK 7°/0° 14x18x05mm
8825-0705

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3014
In Commercial Distribution

  • 00888480572527 ()

  • TLIF CHANNELED PEEK 0° 9X30X14MM
8859-3014

  • Polymeric spinal interbody fusion cage
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