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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 Size Type Device Class Implantable

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Interlock II Ti-C, 11x17x14mm 10°
Nuvasive, Inc.
6771110CP2
In Commercial Distribution

  • 00887517812582 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 10x17x14mm 10°
Nuvasive, Inc.
6771010CP2
In Commercial Distribution

  • 00887517812537 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 9x17x14mm 10°
Nuvasive, Inc.
6770910CP2
In Commercial Distribution

  • 00887517812483 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 8x17x14mm 10°
Nuvasive, Inc.
6770810CP2
In Commercial Distribution

  • 00887517812445 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 7x17x14mm 10°
Nuvasive, Inc.
6770710CP2
In Commercial Distribution

  • 00887517812414 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W Ti-C, 16x22x60mm 10°
Nuvasive, Inc.
6921660CP2
In Commercial Distribution

  • 00887517817068 ()


  • Metal-polymer composite spinal interbody fusion cage
CoRoent XL-W Ti-C, 16x22x55mm 10°
Nuvasive, Inc.
6921655CP2
In Commercial Distribution

  • 00887517817051 ()


  • Metal-polymer composite spinal interbody fusion cage
CoRoent XL-W Ti-C, 16x22x50mm 10°
Nuvasive, Inc.
6921650CP2
In Commercial Distribution

  • 00887517817044 ()


  • Metal-polymer composite spinal interbody fusion cage
CoRoent XL-W Ti-C, 16x22x45mm 10°
Nuvasive, Inc.
6921645CP2
In Commercial Distribution

  • 00887517817037 ()


  • Metal-polymer composite spinal interbody fusion cage
CoRoent XL-W Ti-C, 14x22x60mm 10°
Nuvasive, Inc.
6921460CP2
In Commercial Distribution

  • 00887517817020 ()


  • Metal-polymer composite spinal interbody fusion cage
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