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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TLX Implant, 10x11x31mm 15°
Nuvasive, Inc.
5801305
In Commercial Distribution

  • 00887517729552 ()


  • Metallic spinal fusion cage, non-sterile
TLX Implant, 10x11x26mm 15°
Nuvasive, Inc.
5801255
In Commercial Distribution

  • 00887517729538 ()


  • Metallic spinal fusion cage, non-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, 8x22x45mm 10°
Nuvasive, Inc.
6308245P
In Commercial Distribution

  • 00887517227348 ()


  • 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+, 8x18x50mm 10°
Nuvasive, Inc.
6308850P
In Commercial Distribution

  • 00887517224637 ()


  • Polymeric spinal fusion cage, sterile
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