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
8824-4312
In Commercial Distribution

  • 00887868211478 ()

  • ACDF PEEK 0° 14x18x12mm
8824-4312

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4311
In Commercial Distribution

  • 00887868211461 ()

  • ACDF PEEK 0° 14x18x11mm
8824-4311

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4310
In Commercial Distribution

  • 00887868211454 ()

  • ACDF PEEK 0° 14x18x10mm
8824-4310

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8824-4309
In Commercial Distribution

  • 00887868211447 ()

  • ACDF PEEK 0° 14x18x9mm
8824-4309

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1238
In Commercial Distribution

  • 00887868210945 ()

  • VBR PEEK 0° 12x14x38mm
8804-1238

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1235
In Commercial Distribution

  • 00887868210921 ()

  • VBR PEEK 0° 12x14x35mm
8804-1235

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1232
In Commercial Distribution

  • 00887868210907 ()

  • VBR PEEK 0° 12x14x32mm
8804-1232

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1226
In Commercial Distribution

  • 00887868210877 ()

  • VBR PEEK 0° 12x14x26mm
8804-1226

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1222
In Commercial Distribution

  • 00887868210846 ()

  • VBR PEEK 0° 12x14x22mm
8804-1222

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1218
In Commercial Distribution

  • 00887868210822 ()

  • VBR PEEK 0° 12x14x18mm
8804-1218

  • Polymeric spinal interbody fusion cage
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