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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 Class Implantable

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CoRoent XL+, 12x18x55mm
Nuvasive, Inc.
6012855P2
In Commercial Distribution

  • 00887517992987 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 12x18x50mm
Nuvasive, Inc.
6012850P2
In Commercial Distribution

  • 00887517992970 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 12x18x45mm
Nuvasive, Inc.
6012845P2
In Commercial Distribution

  • 00887517992963 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 11x18x60mm
Nuvasive, Inc.
6011860P2
In Commercial Distribution

  • 00887517992956 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 11x18x55mm
Nuvasive, Inc.
6011855P2
In Commercial Distribution

  • 00887517992949 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 11x18x50mm
Nuvasive, Inc.
6011850P2
In Commercial Distribution

  • 00887517992932 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 11x18x45mm
Nuvasive, Inc.
6011845P2
In Commercial Distribution

  • 00887517992925 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 9x18x60mm
Nuvasive, Inc.
6009860P2
In Commercial Distribution

  • 00887517992918 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 9x18x55mm
Nuvasive, Inc.
6009855P2
In Commercial Distribution

  • 00887517992901 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 9x18x50mm
Nuvasive, Inc.
6009850P2
In Commercial Distribution

  • 00887517992895 ()


  • Polymeric spinal fusion cage, sterile
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