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-W+, 10x22x55mm 10°
Nuvasive, Inc.
6310255
In Commercial Distribution

  • 00887517306517 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x50mm 10°
Nuvasive, Inc.
6310250
In Commercial Distribution

  • 00887517306500 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x45mm 10°
Nuvasive, Inc.
6310245
In Commercial Distribution

  • 00887517306296 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 10x22x40mm 10°
Nuvasive, Inc.
6310240
In Commercial Distribution

  • 00887517306289 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x60mm 10°
Nuvasive, Inc.
6309260
In Commercial Distribution

  • 00887517305855 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x55mm 10°
Nuvasive, Inc.
6309255
In Commercial Distribution

  • 00887517305848 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x50mm 10°
Nuvasive, Inc.
6309250
In Commercial Distribution

  • 00887517305831 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x45mm 10°
Nuvasive, Inc.
6309245
In Commercial Distribution

  • 00887517305824 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x60mm 10°
Nuvasive, Inc.
6308860
In Commercial Distribution

  • 00887517305497 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL+, 8x18x55mm 10°
Nuvasive, Inc.
6308855
In Commercial Distribution

  • 00887517305480 ()


  • Polymeric spinal interbody fusion cage
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