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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 - 00887517377210

CoRoent® LO, 8x10x25mm 5°
Nuvasive, Inc.
6850810
In Commercial Distribution

  • 00887517377210 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722904

CoRoent LO Ti, 14x10x40mm 5°
Nuvasive, Inc.
6081440P2
In Commercial Distribution

  • 00887517722904 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722898

CoRoent LO Ti, 14x10x35mm 5°
Nuvasive, Inc.
6081435P2
In Commercial Distribution

  • 00887517722898 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722881

CoRoent LO Ti, 14x10x30mm 5°
Nuvasive, Inc.
6081430P2
In Commercial Distribution

  • 00887517722881 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722874

CoRoent LO Ti, 14x10x25mm 5°
Nuvasive, Inc.
6081425P2
In Commercial Distribution

  • 00887517722874 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722867

CoRoent LO Ti, 12x10x40mm 5°
Nuvasive, Inc.
6081240P2
In Commercial Distribution

  • 00887517722867 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722850

CoRoent LO Ti, 12x10x35mm 5°
Nuvasive, Inc.
6081235P2
In Commercial Distribution

  • 00887517722850 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722843

CoRoent LO Ti, 12x10x30mm 5°
Nuvasive, Inc.
6081230P2
In Commercial Distribution

  • 00887517722843 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722836

CoRoent LO Ti, 12x10x25mm 5°
Nuvasive, Inc.
6081225P2
In Commercial Distribution

  • 00887517722836 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722829

CoRoent LO Ti, 10x10x40mm 5°
Nuvasive, Inc.
6081040P2
In Commercial Distribution

  • 00887517722829 ()


  • Polymeric spinal interbody fusion cage
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