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
8824-4305
In Commercial Distribution

  • 00887868211409 ()

  • ACDF PEEK 0° 14x18x5mm
8824-4305

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4211
In Commercial Distribution

  • 00887868211386 ()

  • ACDF PEEK 0° 13x16x11mm
8824-4211

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4209
In Commercial Distribution

  • 00887868211362 ()

  • ACDF PEEK 0° 13x16x9mm
8824-4209

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4207
In Commercial Distribution

  • 00887868211348 ()

  • ACDF PEEK 0° 13x16x7mm
8824-4207

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4206
In Commercial Distribution

  • 00887868211331 ()

  • ACDF PEEK 0° 13x16x6mm
8824-4206

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4205
In Commercial Distribution

  • 00887868211324 ()

  • ACDF PEEK 0° 13x16x5mm
8824-4205

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4111
In Commercial Distribution

  • 00887868211300 ()

  • ACDF PEEK 0° 12x14x11mm
8824-4111

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4106
In Commercial Distribution

  • 00887868211256 ()

  • ACDF PEEK 0° 12x14x6mm
8824-4106

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1250
In Commercial Distribution

  • 00887868211010 ()

  • VBR PEEK 0° 12x14x50mm
8804-1250

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1245
In Commercial Distribution

  • 00887868210983 ()

  • VBR PEEK 0° 12x14x45mm
8804-1245

  • Polymeric spinal interbody fusion cage
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