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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 - 00887517722843

CoRoent LO Ti, 12x10x30mm 5°
Nuvasive, Inc.
6081230P2
In Commercial Distribution

  • 00887517722843 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722836

CoRoent LO Ti, 12x10x25mm 5°
Nuvasive, Inc.
6081225P2
In Commercial Distribution

  • 00887517722836 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722829

CoRoent LO Ti, 10x10x40mm 5°
Nuvasive, Inc.
6081040P2
In Commercial Distribution

  • 00887517722829 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722812

CoRoent LO Ti, 10x10x35mm 5°
Nuvasive, Inc.
6081035P2
In Commercial Distribution

  • 00887517722812 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722805

CoRoent LO Ti, 10x10x30mm 5°
Nuvasive, Inc.
6081030P2
In Commercial Distribution

  • 00887517722805 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722799

CoRoent LO Ti, 10x10x25mm 5°
Nuvasive, Inc.
6081025P2
In Commercial Distribution

  • 00887517722799 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722782

CoRoent LO Ti, 8x10x40mm 5°
Nuvasive, Inc.
6080840P2
In Commercial Distribution

  • 00887517722782 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722775

CoRoent LO Ti, 8x10x35mm 5°
Nuvasive, Inc.
6080835P2
In Commercial Distribution

  • 00887517722775 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722768

CoRoent LO Ti, 8x10x30mm 5°
Nuvasive, Inc.
6080830P2
In Commercial Distribution

  • 00887517722768 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517722751

CoRoent LO Ti, 8x10x25mm 5°
Nuvasive, Inc.
6080825P2
In Commercial Distribution

  • 00887517722751 ()


  • Polymeric spinal interbody fusion cage
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