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
8804-1216
In Commercial Distribution

  • 00887868210815 ()

  • VBR PEEK 0° 12x14x16mm
8804-1216

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1215
In Commercial Distribution

  • 00887868210808 ()

  • VBR PEEK 0° 12x14x15mm
8804-1215

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1214
In Commercial Distribution

  • 00887868210792 ()

  • VBR PEEK 0° 12x14x14mm
8804-1214

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8804-1213
In Commercial Distribution

  • 00887868210785 ()

  • VBR PEEK 0° 12x14x13mm
8804-1213

  • 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
No Description
BIOMET SPINE LLC
8880-0208
In Commercial Distribution

  • 00887868213458 ()

  • ALIF PEEK 0° 27x36x8mm
8880-0208

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0116
In Commercial Distribution

  • 00887868213427 ()

  • ALIF PEEK 0° 24x32x16mm
8880-0116

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8880-0112
In Commercial Distribution

  • 00887868213403 ()

  • ALIF PEEK 0° 24x32x12mm
8880-0112

  • Polymeric spinal interbody fusion cage
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