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 Device Size Type Device Class Implantable

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CoRoent Large MP, 11x9x23mm 0°
Nuvasive, Inc.
6001123P2
In Commercial Distribution

  • 00887517678508 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 10x9x28mm 0°
Nuvasive, Inc.
6001028P2
In Commercial Distribution

  • 00887517678485 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 10x9x23mm 0°
Nuvasive, Inc.
6001023P2
In Commercial Distribution

  • 00887517678461 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 9x9x28mm 0°
Nuvasive, Inc.
6000928P2
In Commercial Distribution

  • 00887517678447 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 9x9x23mm 0°
Nuvasive, Inc.
6000923P2
In Commercial Distribution

  • 00887517678423 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 8x9x28mm 0°
Nuvasive, Inc.
6000828P2
In Commercial Distribution

  • 00887517678409 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 8x9x23mm 0°
Nuvasive, Inc.
6000823P2
In Commercial Distribution

  • 00887517678386 ()


  • Polymeric spinal interbody fusion cage
TLX Expanding Trial, 7-13mm
Nuvasive, Inc.
1775170
In Commercial Distribution

  • 00887517671837 ()


  • Spinal implant trial
CoRoent Ant TLIF Ti, 7x9x40mm 8°
Nuvasive, Inc.
5279408
In Commercial Distribution

  • 00887517660459 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 7x9x40mm 4°
Nuvasive, Inc.
5279404
In Commercial Distribution

  • 00887517660442 ()


  • Polymeric spinal interbody fusion cage
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