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

Show Filters

No Description
BIOMET SPINE LLC
8825-0746
In Commercial Distribution

  • 00888480571445 ()

  • VBR PEEK 7°/0° 14X18X46MM
8825-0746

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

  • 00888480571438 ()

  • VBR PEEK 7°/0° 14X18X45MM
8825-0745

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0744
In Commercial Distribution

  • 00888480571421 ()

  • VBR PEEK 7°/0° 14X18X44MM
8825-0744

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0743
In Commercial Distribution

  • 00888480571414 ()

  • VBR PEEK 7°/0° 14X18X43MM
8825-0743

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0742
In Commercial Distribution

  • 00888480571407 ()

  • VBR PEEK 7°/0° 14X18X42MM
8825-0742

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0741
In Commercial Distribution

  • 00888480571391 ()

  • VBR PEEK 7°/0° 14X18X41MM
8825-0741

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0740
In Commercial Distribution

  • 00888480571384 ()

  • VBR PEEK 7°/0° 14X18X40MM
8825-0740

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0739
In Commercial Distribution

  • 00888480571377 ()

  • VBR PEEK 7°/0° 14X18X39MM
8825-0739

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

  • 00888480571360 ()

  • VBR PEEK 7°/0° 14X18X38MM
8825-0738

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8825-0737
In Commercial Distribution

  • 00888480571353 ()

  • VBR PEEK 7°/0° 14X18X37MM
8825-0737

  • Polymeric spinal interbody fusion cage
< 1 ... 35 36 37 38 39 ... 153 >