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

  • 00887517722829 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 10x10x35mm 5°
Nuvasive, Inc.
6081035P2
In Commercial Distribution

  • 00887517722812 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 10x10x30mm 5°
Nuvasive, Inc.
6081030P2
In Commercial Distribution

  • 00887517722805 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 10x10x25mm 5°
Nuvasive, Inc.
6081025P2
In Commercial Distribution

  • 00887517722799 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 8x10x40mm 5°
Nuvasive, Inc.
6080840P2
In Commercial Distribution

  • 00887517722782 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 8x10x35mm 5°
Nuvasive, Inc.
6080835P2
In Commercial Distribution

  • 00887517722775 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 8x10x30mm 5°
Nuvasive, Inc.
6080830P2
In Commercial Distribution

  • 00887517722768 ()


  • Polymeric spinal interbody fusion cage
CoRoent LO Ti, 8x10x25mm 5°
Nuvasive, Inc.
6080825P2
In Commercial Distribution

  • 00887517722751 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LO, 14x10x25mm 5°
Nuvasive, Inc.
6851410
In Commercial Distribution

  • 00887517379108 ()


  • Polymeric spinal interbody fusion cage
CoRoent® LO, 13x10x30mm 5°
Nuvasive, Inc.
6851311
In Commercial Distribution

  • 00887517378842 ()


  • Polymeric spinal interbody fusion cage
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