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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 - 00887517295057

CoRoent® XL-H, 2x22x50mm 20°
Nuvasive, Inc.
6200250
In Commercial Distribution

  • 00887517295057 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517295040

CoRoent® XL-H, 2x22x45mm 20°
Nuvasive, Inc.
6200245
In Commercial Distribution

  • 00887517295040 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517293152

CoRoent® XLFW, 14x22x60mm Lordotic
Nuvasive, Inc.
6171460
In Commercial Distribution

  • 00887517293152 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517293145

CoRoent® XLFW, 14x22x55mm Lordotic
Nuvasive, Inc.
6171455
In Commercial Distribution

  • 00887517293145 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517293138

CoRoent® XLFW, 14x22x50mm Lordotic
Nuvasive, Inc.
6171450
In Commercial Distribution

  • 00887517293138 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517293114

CoRoent® XLFW, 12x22x60mm Lordotic
Nuvasive, Inc.
6171260
In Commercial Distribution

  • 00887517293114 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517293107

CoRoent® XLFW, 12x22x55mm Lordotic
Nuvasive, Inc.
6171255
In Commercial Distribution

  • 00887517293107 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292797

CoRoent® XLFW, 12x22x50mm Lordotic
Nuvasive, Inc.
6171250
In Commercial Distribution

  • 00887517292797 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292780

CoRoent® XLFW, 12x22x45mm Lordotic
Nuvasive, Inc.
6171245
In Commercial Distribution

  • 00887517292780 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517292773

CoRoent® XLFW, 10x22x60mm Lordotic
Nuvasive, Inc.
6171060
In Commercial Distribution

  • 00887517292773 ()


  • Polymeric spinal interbody fusion cage
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