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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 Class Implantable

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CoRoent® XL+, 8x18x50mm 10°
Nuvasive, Inc.
6308850P
In Commercial Distribution

  • 00887517224637 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 10x18x45mm 10°
Nuvasive, Inc.
6310845P
In Commercial Distribution

  • 00887517224262 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 8x18x45mm 10°
Nuvasive, Inc.
6308845P
In Commercial Distribution

  • 00887517224248 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 10x18x60mm
Nuvasive, Inc.
6010860P
In Commercial Distribution

  • 00887517223876 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 8x18x60mm
Nuvasive, Inc.
6008860P
In Commercial Distribution

  • 00887517223852 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 10x18x55mm
Nuvasive, Inc.
6010855P
In Commercial Distribution

  • 00887517223364 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 8x18x55mm
Nuvasive, Inc.
6008855P
In Commercial Distribution

  • 00887517223340 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 10x18x50mm
Nuvasive, Inc.
6010850P
In Commercial Distribution

  • 00887517222954 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 8x18x50mm
Nuvasive, Inc.
6008850P
In Commercial Distribution

  • 00887517222930 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 10x18x45mm
Nuvasive, Inc.
6010845P
In Commercial Distribution

  • 00887517222541 ()


  • Polymeric spinal fusion cage, sterile
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