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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 - 00887517737168

CoRoent LO Ti, 15x10x25mm 5°
Nuvasive, Inc.
6081525P2
In Commercial Distribution

  • 00887517737168 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737151

CoRoent LO Ti, 13x10x40mm 5°
Nuvasive, Inc.
6081340P2
In Commercial Distribution

  • 00887517737151 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737144

CoRoent LO Ti, 13x10x35mm 5°
Nuvasive, Inc.
6081335P2
In Commercial Distribution

  • 00887517737144 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737137

CoRoent LO Ti, 13x10x30mm 5°
Nuvasive, Inc.
6081330P2
In Commercial Distribution

  • 00887517737137 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737120

CoRoent LO Ti, 13x10x25mm 5°
Nuvasive, Inc.
6081325P2
In Commercial Distribution

  • 00887517737120 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737113

CoRoent LO Ti, 11x10x40mm 5°
Nuvasive, Inc.
6081140P2
In Commercial Distribution

  • 00887517737113 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737106

CoRoent LO Ti, 11x10x35mm 5°
Nuvasive, Inc.
6081135P2
In Commercial Distribution

  • 00887517737106 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737090

CoRoent LO Ti, 11x10x30mm 5°
Nuvasive, Inc.
6081130P2
In Commercial Distribution

  • 00887517737090 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737083

CoRoent LO Ti, 11x10x25mm 5°
Nuvasive, Inc.
6081125P2
In Commercial Distribution

  • 00887517737083 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737076

CoRoent LO Ti, 9x10x40mm 5°
Nuvasive, Inc.
6080940P2
In Commercial Distribution

  • 00887517737076 ()


  • Polymeric spinal interbody fusion cage
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