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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 - 00887517272744

CoRoent Large MP, 12x9x23mm 4°
Nuvasive, Inc.
6004235
In Commercial Distribution

  • 00887517272744 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517272737

CoRoent Large MP, 10x9x23mm 4°
Nuvasive, Inc.
6004233
In Commercial Distribution

  • 00887517272737 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517272720

CoRoent Large MP, 8x9x23mm 4°
Nuvasive, Inc.
6004231
In Commercial Distribution

  • 00887517272720 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313683

CoRoent® XL-W+, 10x22x60mm
Nuvasive, Inc.
6510260
In Commercial Distribution

  • 00887517313683 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313676

CoRoent® XL-W+, 10x22x55mm
Nuvasive, Inc.
6510255
In Commercial Distribution

  • 00887517313676 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313669

CoRoent® XL-W+, 10x22x50mm
Nuvasive, Inc.
6510250
In Commercial Distribution

  • 00887517313669 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313652

CoRoent® XL-W+, 10x22x45mm
Nuvasive, Inc.
6510245
In Commercial Distribution

  • 00887517313652 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313645

CoRoent® XL-W+, 10x22x40mm
Nuvasive, Inc.
6510240
In Commercial Distribution

  • 00887517313645 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313263

CoRoent® XL-W+, 8x22x60mm
Nuvasive, Inc.
6508260
In Commercial Distribution

  • 00887517313263 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517313256

CoRoent® XL-W+, 8x22x55mm
Nuvasive, Inc.
6508255
In Commercial Distribution

  • 00887517313256 ()


  • Polymeric spinal interbody fusion cage
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