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
8412-0010
In Commercial Distribution

  • 00887868193668 ()

  • ACDF PEEK 0° 14x17x10mm
8412-0010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0008
In Commercial Distribution

  • 00887868193644 ()

  • ACDF PEEK 0° 14x17x8mm
8412-0008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0006
In Commercial Distribution

  • 00887868193620 ()

  • ACDF PEEK 0° 14x17x6mm
8412-0006

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0005
In Commercial Distribution

  • 00887868193613 ()

  • ACDF PEEK 0° 14x17x5mm
8412-0005

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0012
In Commercial Distribution

  • 00887868193446 ()

  • ACDF PEEK 0° 13x15x12mm
8411-0012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0010
In Commercial Distribution

  • 00887868193422 ()

  • ACDF PEEK 0° 13x15x10mm
8411-0010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0008
In Commercial Distribution

  • 00887868193408 ()

  • ACDF PEEK 0° 13x15x8mm
8411-0008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0006
In Commercial Distribution

  • 00887868193385 ()

  • ACDF PEEK 0° 13x15x6mm
8411-0006

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0218
In Commercial Distribution

  • 00887868213502 ()

  • ALIF PEEK 0° 27x36x18mm
8880-0218

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0214
In Commercial Distribution

  • 00887868213489 ()

  • ALIF PEEK 0° 27x36x14mm
8880-0214

  • Polymeric spinal interbody fusion cage
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