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-XW Ti-C, 12x26x50mm 10°
Nuvasive, Inc.
6212150CP2
In Commercial Distribution

  • 00887517644800 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-XW Ti-C, 10x26x60mm 10°
Nuvasive, Inc.
6210160CP2
In Commercial Distribution

  • 00887517644794 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-XW Ti-C, 10x26x55mm 10°
Nuvasive, Inc.
6210155CP2
In Commercial Distribution

  • 00887517644787 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-XW Ti-C, 10x26x50mm 10°
Nuvasive, Inc.
6210150CP2
In Commercial Distribution

  • 00887517644770 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-XW Ti-C, 8x26x60mm 10°
Nuvasive, Inc.
6208160CP2
In Commercial Distribution

  • 00887517644763 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-XW Ti-C, 8x26x55mm 10°
Nuvasive, Inc.
6208155CP2
In Commercial Distribution

  • 00887517644756 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-XW Ti-C, 8x26x50mm 10°
Nuvasive, Inc.
6208150CP2
In Commercial Distribution

  • 00887517644749 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W Ti-C, 12x22x60mm 10°
Nuvasive, Inc.
6921260CP2
In Commercial Distribution

  • 00887517644695 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W Ti-C, 12x22x55mm 10°
Nuvasive, Inc.
6921255CP2
In Commercial Distribution

  • 00887517644688 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL-W Ti-C, 12x22x50mm 10°
Nuvasive, Inc.
6921250CP2
In Commercial Distribution

  • 00887517644671 ()


  • Polymeric spinal fusion cage, sterile
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