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 Ant TLIF Ti, 11x14x36mm 0°
Nuvasive, Inc.
5214360
In Commercial Distribution

  • 00887517576569 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x40mm 8°
Nuvasive, Inc.
5199408
In Commercial Distribution

  • 00887517576552 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x40mm 4°
Nuvasive, Inc.
5199404
In Commercial Distribution

  • 00887517576545 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x40mm 0°
Nuvasive, Inc.
5199400
In Commercial Distribution

  • 00887517576538 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x36mm 8°
Nuvasive, Inc.
5199368
In Commercial Distribution

  • 00887517576521 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x36mm 4°
Nuvasive, Inc.
5199364
In Commercial Distribution

  • 00887517576514 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x36mm 0°
Nuvasive, Inc.
5199360
In Commercial Distribution

  • 00887517576507 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x40mm 8°
Nuvasive, Inc.
5193408
In Commercial Distribution

  • 00887517576491 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x40mm 4°
Nuvasive, Inc.
5193404
In Commercial Distribution

  • 00887517576484 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x40mm 0°
Nuvasive, Inc.
5193400
In Commercial Distribution

  • 00887517576477 ()


  • Polymeric spinal interbody fusion cage
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