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
8858-3012
In Commercial Distribution

  • 00888480572428 ()

  • TLIF THREADED PEEK 0° 9X30X12MM
8858-3012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-3011
In Commercial Distribution

  • 00888480572411 ()

  • TLIF THREADED PEEK 0° 9X30X11MM
8858-3011

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-3010
In Commercial Distribution

  • 00888480572404 ()

  • TLIF THREADED PEEK 0° 9X30X10MM
8858-3010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-3009
In Commercial Distribution

  • 00888480572398 ()

  • TLIF THREADED PEEK 0° 9X30X9MM
8858-3009

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-3008
In Commercial Distribution

  • 00888480572381 ()

  • TLIF THREADED PEEK 0° 9X30X8MM
8858-3008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-3007
In Commercial Distribution

  • 00888480572374 ()

  • TLIF THREADED PEEK 0° 9X30X7MM
8858-3007

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2514
In Commercial Distribution

  • 00888480572367 ()

  • TLIF THREADED PEEK 0° 9X25X14MM
8858-2514

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2513
In Commercial Distribution

  • 00888480572350 ()

  • TLIF THREADED PEEK 0° 9X25X13MM
8858-2513

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2512
In Commercial Distribution

  • 00888480572343 ()

  • TLIF THREADED PEEK 0° 9X25X12MM
8858-2512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2511
In Commercial Distribution

  • 00888480572336 ()

  • TLIF THREADED PEEK 0° 9X25X11MM
8858-2511

  • Polymeric spinal interbody fusion cage
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