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
8825-0720
In Commercial Distribution

  • 00887868212031 ()

  • VBR PEEK 7°/0° 14x18x20mm
8825-0720

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0718
In Commercial Distribution

  • 00887868212017 ()

  • VBR PEEK 7°/0° 14x18x18mm
8825-0718

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0714
In Commercial Distribution

  • 00887868211973 ()

  • VBR PEEK 7°/0° 14x18x14mm
8825-0714

  • 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
8825-0712
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
8825-0706
In Commercial Distribution

  • 00887868211898 ()

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

  • Polymeric spinal interbody fusion cage
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
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