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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+ Wide, 8x22x55mm 10°
Nuvasive, Inc.
6308255P
In Commercial Distribution

  • 00887517228222 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+ Wide, 10x22x50mm 10°
Nuvasive, Inc.
6310250P
In Commercial Distribution

  • 00887517227751 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+ Wide, 10x22x45mm 10°
Nuvasive, Inc.
6310245P
In Commercial Distribution

  • 00887517227362 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+ Wide, 10x22x60mm
Nuvasive, Inc.
6510260P
In Commercial Distribution

  • 00887517226976 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+ Wide, 8x22x60mm
Nuvasive, Inc.
6508260P
In Commercial Distribution

  • 00887517226952 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+ Wide, 10x22x55mm
Nuvasive, Inc.
6510255P
In Commercial Distribution

  • 00887517226563 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+ Wide, 8x22x55mm
Nuvasive, Inc.
6508255P
In Commercial Distribution

  • 00887517226549 ()


  • Polymeric spinal fusion cage, sterile
CoRoent® XL+, 10x18x55mm 10°
Nuvasive, Inc.
6310855P
In Commercial Distribution

  • 00887517225047 ()


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

  • 00887517224248 ()


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

  • 00887517223852 ()


  • Polymeric spinal fusion cage, sterile
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