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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 - 00887517813602

Interlock II Ti-C, 15x19x16mm 20°
Nuvasive, Inc.
6779520CP2
In Commercial Distribution

  • 00887517813602 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813541

Interlock II Ti-C, 14x19x16mm 20°
Nuvasive, Inc.
6779420CP2
In Commercial Distribution

  • 00887517813541 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813480

Interlock II Ti-C, 13x19x16mm 20°
Nuvasive, Inc.
6779320CP2
In Commercial Distribution

  • 00887517813480 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813428

Interlock II Ti-C, 12x19x16mm 20°
Nuvasive, Inc.
6779220CP2
In Commercial Distribution

  • 00887517813428 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813374

Interlock II Ti-C, 11x19x16mm 20°
Nuvasive, Inc.
6779120CP2
In Commercial Distribution

  • 00887517813374 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813329

Interlock II Ti-C, 10x19x16mm 20°
Nuvasive, Inc.
6779020CP2
In Commercial Distribution

  • 00887517813329 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813282

Interlock II Ti-C, 9x19x16mm 20°
Nuvasive, Inc.
6778920CP2
In Commercial Distribution

  • 00887517813282 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517812902

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

  • 00887517812902 ()


  • 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
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