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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 - 00887517683717

CoRoent LO, 8x10x30mm 5°
Nuvasive, Inc.
6850811P2
In Commercial Distribution

  • 00887517683717 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517682956

CoRoent LC, 14x9x25 8°
Nuvasive, Inc.
6614925P2
In Commercial Distribution

  • 00887517682956 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517682796

CoRoent LC, 10x9x25 8°
Nuvasive, Inc.
6610925P2
In Commercial Distribution

  • 00887517682796 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680280

CoRoent Large MP, 16x9x23mm 12°
Nuvasive, Inc.
6121623P2
In Commercial Distribution

  • 00887517680280 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680242

CoRoent Large MP, 15x9x23mm 12°
Nuvasive, Inc.
6121523P2
In Commercial Distribution

  • 00887517680242 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680204

CoRoent Large MP, 14x9x23mm 12°
Nuvasive, Inc.
6121423P2
In Commercial Distribution

  • 00887517680204 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680082

CoRoent Large MP, 11x9x23mm 12°
Nuvasive, Inc.
6121123P2
In Commercial Distribution

  • 00887517680082 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680044

CoRoent Large MP, 10x9x23mm 12°
Nuvasive, Inc.
6121023P2
In Commercial Distribution

  • 00887517680044 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680020

CoRoent Large MP, 9x9x28mm 12°
Nuvasive, Inc.
6120928P2
In Commercial Distribution

  • 00887517680020 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517680006

CoRoent Large MP, 9x9x23mm 12°
Nuvasive, Inc.
6120923P2
In Commercial Distribution

  • 00887517680006 ()


  • Polymeric spinal interbody fusion cage
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