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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 Class Implantable

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CoRoent - 00887517890399

CoRoent Ant TLIF PEEK, 13x11x30mm 0°
Nuvasive, Inc.
5131300P2
In Commercial Distribution

  • 00887517890399 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890382

CoRoent Ant TLIF PEEK, 13x11x28mm 8°
Nuvasive, Inc.
5131288P2
In Commercial Distribution

  • 00887517890382 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890375

CoRoent Ant TLIF PEEK, 13x11x28mm 15°
Nuvasive, Inc.
5131285P2
In Commercial Distribution

  • 00887517890375 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890368

CoRoent Ant TLIF PEEK, 13x11x28mm 4°
Nuvasive, Inc.
5131284P2
In Commercial Distribution

  • 00887517890368 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890351

CoRoent Ant TLIF PEEK, 13x11x28mm 12°
Nuvasive, Inc.
5131282P2
In Commercial Distribution

  • 00887517890351 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890344

CoRoent Ant TLIF PEEK, 13x11x28mm 0°
Nuvasive, Inc.
5131280P2
In Commercial Distribution

  • 00887517890344 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890337

CoRoent Ant TLIF Ti, 13x10x40mm 8°
Nuvasive, Inc.
5130408P2
In Commercial Distribution

  • 00887517890337 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890320

CoRoent Ant TLIF Ti, 13x10x40mm 4°
Nuvasive, Inc.
5130404P2
In Commercial Distribution

  • 00887517890320 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890313

CoRoent Ant TLIF Ti, 13x10x40mm 0°
Nuvasive, Inc.
5130400P2
In Commercial Distribution

  • 00887517890313 ()


  • Metallic spinal interbody fusion cage

CoRoent - 00887517890306

CoRoent Ant TLIF Ti, 13x10x36mm 8°
Nuvasive, Inc.
5130368P2
In Commercial Distribution

  • 00887517890306 ()


  • Metallic spinal interbody fusion cage
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