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
8858-2514
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
No Description
BIOMET SPINE LLC
8858-2510
In Commercial Distribution

  • 00888480572329 ()

  • TLIF THREADED PEEK 0° 9X25X10MM
8858-2510

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2509
In Commercial Distribution

  • 00888480572312 ()

  • TLIF THREADED PEEK 0° 9X25X9MM
8858-2509

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2508
In Commercial Distribution

  • 00888480572305 ()

  • TLIF THREADED PEEK 0° 9X25X8MM
8858-2508

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8858-2507
In Commercial Distribution

  • 00888480572299 ()

  • TLIF THREADED PEEK 0° 9X25X7MM
8858-2507

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2714
In Commercial Distribution

  • 00888480571803 ()

  • PLIF THREADED PEEK 0° 10X27X14MM
8830-2714

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8830-2713
In Commercial Distribution

  • 00888480571797 ()

  • PLIF THREADED PEEK 0° 10X27X13MM
8830-2713

  • Polymeric spinal interbody fusion cage
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