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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 Large MP, 13x9x23mm 12°
Nuvasive, Inc.
6121323P2
In Commercial Distribution

  • 00887517680167 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 12x9x28mm 12°
Nuvasive, Inc.
6121228P2
In Commercial Distribution

  • 00887517680143 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 12x9x23mm 12°
Nuvasive, Inc.
6121223P2
In Commercial Distribution

  • 00887517680129 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 11x9x28mm 12°
Nuvasive, Inc.
6121128P2
In Commercial Distribution

  • 00887517680105 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 10x9x28mm 12°
Nuvasive, Inc.
6121028P2
In Commercial Distribution

  • 00887517680068 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 13x9x23mm 8°
Nuvasive, Inc.
6081323P2
In Commercial Distribution

  • 00887517679802 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 12x9x28mm 8°
Nuvasive, Inc.
6081228P2
In Commercial Distribution

  • 00887517679789 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 12x9x23mm 8°
Nuvasive, Inc.
6081223P2
In Commercial Distribution

  • 00887517679765 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 11x9x28mm 8°
Nuvasive, Inc.
6081128P2
In Commercial Distribution

  • 00887517679741 ()


  • Polymeric spinal interbody fusion cage
CoRoent Large MP, 11x9x23mm 8°
Nuvasive, Inc.
6081123P2
In Commercial Distribution

  • 00887517679727 ()


  • Polymeric spinal interbody fusion cage
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