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
1400-0002
In Commercial Distribution

  • 00888480185246 ()

  • SOLITAIRE NARROW 12MM / 0°
1400-0002

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
1400-0000
In Commercial Distribution

  • 00888480185239 ()

  • SOLITAIRE NARROW 10MM / 0°
1400-0000

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
07.01707.022
In Commercial Distribution

  • 00889024328013 ()

  • Polyaxial Smooth Shank Screw Ø4.0 mm X 24 mm L
07.01707.022

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8859-3014
In Commercial Distribution

  • 00888480572527 ()

  • TLIF CHANNELED PEEK 0° 9X30X14MM
8859-3014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3012
In Commercial Distribution

  • 00888480572510 ()

  • TLIF CHANNELED PEEK 0° 9X30X12MM
8859-3012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3010
In Commercial Distribution

  • 00888480572503 ()

  • TLIF CHANNELED PEEK 0° 9X30X10MM
8859-3010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-3008
In Commercial Distribution

  • 00888480572497 ()

  • TLIF CHANNELED PEEK 0° 9X30X8MM
8859-3008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-2514
In Commercial Distribution

  • 00888480572480 ()

  • TLIF CHANNELED PEEK 0° 9X25X14MM
8859-2514

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-2512
In Commercial Distribution

  • 00888480572473 ()

  • TLIF CHANNELED PEEK 0° 9X25X12MM
8859-2512

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8859-2510
In Commercial Distribution

  • 00888480572466 ()

  • TLIF CHANNELED PEEK 0° 9X25X10MM
8859-2510

  • Polymeric spinal interbody fusion cage
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