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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 - 00887517681065

CoRoent XL-H, 10x22x60mm 20°
Nuvasive, Inc.
6201060P2
In Commercial Distribution

  • 00887517681065 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517681027

CoRoent XL-H, 10x22x40mm 20°
Nuvasive, Inc.
6201040P2
In Commercial Distribution

  • 00887517681027 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517681010

CoRoent XL-H, 8x22x60mm 20°
Nuvasive, Inc.
6200860P2
In Commercial Distribution

  • 00887517681010 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680976

CoRoent XL-H, 8x22x40mm 20°
Nuvasive, Inc.
6200840P2
In Commercial Distribution

  • 00887517680976 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680969

CoRoent XL-H, 6x22x60mm 20°
Nuvasive, Inc.
6200660P2
In Commercial Distribution

  • 00887517680969 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680921

CoRoent XL-H, 6x22x40mm 20°
Nuvasive, Inc.
6200640P2
In Commercial Distribution

  • 00887517680921 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680914

CoRoent XL-H, 4x22x60mm 20°
Nuvasive, Inc.
6200460P2
In Commercial Distribution

  • 00887517680914 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680877

CoRoent XL-H, 4x22x40mm 20°
Nuvasive, Inc.
6200440P2
In Commercial Distribution

  • 00887517680877 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680860

CoRoent XL-H, 2x22x60mm 20°
Nuvasive, Inc.
6200260P2
In Commercial Distribution

  • 00887517680860 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680853

CoRoent XL-H, 2x22x55mm 20°
Nuvasive, Inc.
6200255P2
In Commercial Distribution

  • 00887517680853 ()


  • Polymeric spinal interbody fusion cage
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