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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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CoRoent - 00887517812902

Interlock II Ti-C, 16x17x14mm 20°
Nuvasive, Inc.
6771620CP2
In Commercial Distribution

  • 00887517812902 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812841

Interlock II Ti-C, 15x17x14mm 20°
Nuvasive, Inc.
6771520CP2
In Commercial Distribution

  • 00887517812841 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812780

Interlock II Ti-C, 14x17x14mm 20°
Nuvasive, Inc.
6771420CP2
In Commercial Distribution

  • 00887517812780 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812728

Interlock II Ti-C, 13x17x14mm 20°
Nuvasive, Inc.
6771320CP2
In Commercial Distribution

  • 00887517812728 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812667

Interlock II Ti-C, 12x17x14mm 20°
Nuvasive, Inc.
6771220CP2
In Commercial Distribution

  • 00887517812667 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812605

Interlock II Ti-C, 11x17x14mm 20°
Nuvasive, Inc.
6771120CP2
In Commercial Distribution

  • 00887517812605 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812551

Interlock II Ti-C, 10x17x14mm 20°
Nuvasive, Inc.
6771020CP2
In Commercial Distribution

  • 00887517812551 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812506

Interlock II Ti-C, 9x17x14mm 20°
Nuvasive, Inc.
6770920CP2
In Commercial Distribution

  • 00887517812506 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812469

Interlock II Ti-C, 8x17x14mm 20°
Nuvasive, Inc.
6770820CP2
In Commercial Distribution

  • 00887517812469 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813664

Interlock II Ti-C, 16x19x16mm 20°
Nuvasive, Inc.
6779620CP2
In Commercial Distribution

  • 00887517813664 ()


  • Polymeric spinal interbody fusion cage
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