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
8412-0011
In Commercial Distribution

  • 00887868193675 ()

  • ACDF PEEK 0° 14x17x11mm
8412-0011

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0009
In Commercial Distribution

  • 00887868193651 ()

  • ACDF PEEK 0° 14x17x9mm
8412-0009

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8412-0007
In Commercial Distribution

  • 00887868193637 ()

  • ACDF PEEK 0° 14x17x7mm
8412-0007

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0011
In Commercial Distribution

  • 00887868193439 ()

  • ACDF PEEK 0° 13x15x11mm
8411-0011

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0009
In Commercial Distribution

  • 00887868193415 ()

  • ACDF PEEK 0° 13x15x9mm
8411-0009

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0007
In Commercial Distribution

  • 00887868193392 ()

  • ACDF PEEK 0° 13x15x7mm
8411-0007

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8411-0005
In Commercial Distribution

  • 00887868193378 ()

  • ACDF PEEK 0° 13x15x5mm
8411-0005

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0220
In Commercial Distribution

  • 00887868213519 ()

  • ALIF PEEK 0° 27x36x20mm
8880-0220

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0216
In Commercial Distribution

  • 00887868213496 ()

  • ALIF PEEK 0° 27x36x16mm
8880-0216

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0212
In Commercial Distribution

  • 00887868213472 ()

  • ALIF PEEK 0° 27x36x12mm
8880-0212

  • Polymeric spinal interbody fusion cage
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