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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 XL+, 12x18x60mm 10°
Nuvasive, Inc.
6312860P2
In Commercial Distribution

  • 00887517993434 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x50mm 10°
Nuvasive, Inc.
6312850P2
In Commercial Distribution

  • 00887517993410 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 12x18x45mm 10°
Nuvasive, Inc.
6312845P2
In Commercial Distribution

  • 00887517993403 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 12x22x60mm 10°
Nuvasive, Inc.
6312260P2
In Commercial Distribution

  • 00887517993397 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 12x22x50mm 10°
Nuvasive, Inc.
6312250P2
In Commercial Distribution

  • 00887517993373 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 11x18x50mm 10°
Nuvasive, Inc.
6311850P2
In Commercial Distribution

  • 00887517993335 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 11x22x55mm 10°
Nuvasive, Inc.
6311255P2
In Commercial Distribution

  • 00887517993304 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 11x22x45mm 10°
Nuvasive, Inc.
6311245P2
In Commercial Distribution

  • 00887517993281 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 9x18x55mm 10°
Nuvasive, Inc.
6309855P2
In Commercial Distribution

  • 00887517993267 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 9x18x45mm 10°
Nuvasive, Inc.
6309845P2
In Commercial Distribution

  • 00887517993243 ()


  • Polymeric spinal interbody fusion cage
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