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
8721-4014
In Commercial Distribution

  • 00887868206269 ()

  • Spacer Lat PEEK 0° 40L X 22W X 14H
8721-4014

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-4012
In Commercial Distribution

  • 00887868206252 ()

  • Spacer Lat PEEK 0° 40L X 22W X 12H
8721-4012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-4010
In Commercial Distribution

  • 00887868206245 ()

  • Spacer Lat PEEK 0° 40L X 22W X 10H
8721-4010

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8721-4008
In Commercial Distribution

  • 00887868206238 ()

  • Spacer Lat PEEK 0° 40L X 22W X 08H
8721-4008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
102M3315
In Commercial Distribution

  • 00880304864023 ()

  • Curved Titanium Spacer Parallel 33L x 15H x 11W 0°
102M3315

  • Spinal implant trial
No Description
BIOMET SPINE LLC
102M3314
In Commercial Distribution

  • 00880304864016 ()

  • Curved Titanium Spacer Parallel 33L x 14H x 11W 0°
102M3314

  • Spinal implant trial
No Description
BIOMET SPINE LLC
102M3313
In Commercial Distribution

  • 00880304864009 ()

  • Curved Titanium Spacer Parallel 33L x 13H x 11W 0°
102M3313

  • Spinal implant trial
No Description
BIOMET SPINE LLC
102M3312
In Commercial Distribution

  • 00880304863996 ()

  • Curved Titanium Spacer Parallel 33L x 12H x 10W 0°
102M3312

  • Spinal implant trial
No Description
BIOMET SPINE LLC
102M3311
In Commercial Distribution

  • 00880304863989 ()

  • Curved Titanium Spacer Parallel 33L x 11H x 10W 0°
102M3311

  • Spinal implant trial
No Description
BIOMET SPINE LLC
102M3310
In Commercial Distribution

  • 00880304863972 ()

  • Curved Titanium Spacer Parallel 33L x 10H x 10W 0°
102M3310

  • Spinal implant trial
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