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
14-533009
In Commercial Distribution

  • 00888480469889 ()

  • CURVE TRIAL 9HX27L 0 DEG 20 DEG ANGLE
14-533009

  • Spinal implant trial
No Description
BIOMET SPINE LLC
14-533008
In Commercial Distribution

  • 00888480469872 ()

  • CURVE TRIAL 8HX27L 0 DEG 20 DEG ANGLE
14-533008

  • Spinal implant trial
No Description
BIOMET SPINE LLC
14-533007
In Commercial Distribution

  • 00888480469865 ()

  • CURVE TRIAL 7HX27L 0 DEG 20 DEG ANGLE
14-533007

  • Spinal implant trial
No Description
BIOMET SPINE LLC
14-533006
In Commercial Distribution

  • 00888480469858 ()

  • CURVE TRIAL 6HX27L 0 DEG 20 DEG ANGLE
14-533006

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8721-6050
In Commercial Distribution

  • 00887868206870 ()

  • Spacer Lat PEEK 0° 60L X 22W X 50H
8721-6050

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-6045
In Commercial Distribution

  • 00887868206863 ()

  • Spacer Lat PEEK 0° 60L X 22W X 45H
8721-6045

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-6040
In Commercial Distribution

  • 00887868206856 ()

  • Spacer Lat PEEK 0° 60L X 22W X 40H
8721-6040

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-6035
In Commercial Distribution

  • 00887868206849 ()

  • Spacer Lat PEEK 0° 60L X 22W X 35H
8721-6035

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-6030
In Commercial Distribution

  • 00887868206832 ()

  • Spacer Lat PEEK 0° 60L X 22W X 30H
8721-6030

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-6025
In Commercial Distribution

  • 00887868206825 ()

  • Spacer Lat PEEK 0° 60L X 22W X 25H
8721-6025

  • Polymeric spinal interbody fusion cage
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