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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 - 00887517292759

CoRoent® XLFW, 10x22x50mm Lordotic
Nuvasive, Inc.
6171050
In Commercial Distribution

  • 00887517292759 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292742

CoRoent® XLFW, 10x22x45mm Lordotic
Nuvasive, Inc.
6171045
In Commercial Distribution

  • 00887517292742 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292735

CoRoent® XLFW, 8x22x60mm Lordotic
Nuvasive, Inc.
6170860
In Commercial Distribution

  • 00887517292735 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292728

CoRoent® XLFW, 8x22x55mm Lordotic
Nuvasive, Inc.
6170855
In Commercial Distribution

  • 00887517292728 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292711

CoRoent® XLFW, 8x22x50mm Lordotic
Nuvasive, Inc.
6170850
In Commercial Distribution

  • 00887517292711 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292704

CoRoent® XLFW, 8x22x45mm Lordotic
Nuvasive, Inc.
6170845
In Commercial Distribution

  • 00887517292704 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292391

CoRoent® XLFW, 14x22x60mm
Nuvasive, Inc.
6161460
In Commercial Distribution

  • 00887517292391 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292384

CoRoent® XLFW, 14x22x55mm
Nuvasive, Inc.
6161455
In Commercial Distribution

  • 00887517292384 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292377

CoRoent® XLFW, 14x22x50mm
Nuvasive, Inc.
6161450
In Commercial Distribution

  • 00887517292377 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292353

CoRoent® XLFW, 12x22x60mm
Nuvasive, Inc.
6161260
In Commercial Distribution

  • 00887517292353 ()


  • Polymeric spinal interbody fusion cage
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