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+, 8x18x55mm
Nuvasive, Inc.
6008855P2
In Commercial Distribution

  • 00887517708014 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 8x18x50mm
Nuvasive, Inc.
6008850P2
In Commercial Distribution

  • 00887517708007 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 8x18x45mm
Nuvasive, Inc.
6008845P2
In Commercial Distribution

  • 00887517707994 ()


  • Polymeric spinal fusion cage, sterile
CoRoent XL+, 8x18x40mm
Nuvasive, Inc.
6008840P2
In Commercial Distribution

  • 00887517707987 ()


  • Polymeric spinal fusion cage, sterile
CoRoent LO, 14x10x35mm 5°
Nuvasive, Inc.
6851412P2
In Commercial Distribution

  • 00887517684097 ()


  • Polymeric spinal fusion cage, sterile
CoRoent LO, 14x10x30mm 5°
Nuvasive, Inc.
6851411P2
In Commercial Distribution

  • 00887517684073 ()


  • Polymeric spinal fusion cage, sterile
CoRoent LO, 14x10x25mm 5°
Nuvasive, Inc.
6851410P2
In Commercial Distribution

  • 00887517684059 ()


  • Polymeric spinal fusion cage, sterile
CoRoent LO, 12x10x35mm 5°
Nuvasive, Inc.
6851212P2
In Commercial Distribution

  • 00887517683977 ()


  • Polymeric spinal fusion cage, sterile
CoRoent LO, 12x10x30mm 5°
Nuvasive, Inc.
6851211P2
In Commercial Distribution

  • 00887517683953 ()


  • Polymeric spinal fusion cage, sterile
CoRoent LO, 12x10x25mm 5°
Nuvasive, Inc.
6851210P2
In Commercial Distribution

  • 00887517683939 ()


  • Polymeric spinal fusion cage, sterile
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