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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 - 00887517810038

Interlock II, 13x17x14mm 30°
Nuvasive, Inc.
6771330
In Commercial Distribution

  • 00887517810038 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517810014

Interlock II, 13x17x14mm 25°
Nuvasive, Inc.
6771325
In Commercial Distribution

  • 00887517810014 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809995

Interlock II, 13x17x14mm 20°
Nuvasive, Inc.
6771320
In Commercial Distribution

  • 00887517809995 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809971

Interlock II, 13x17x14mm 15°
Nuvasive, Inc.
6771315
In Commercial Distribution

  • 00887517809971 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809957

Interlock II, 13x17x14mm 10°
Nuvasive, Inc.
6771310
In Commercial Distribution

  • 00887517809957 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809933

Interlock II, 13x17x14mm 7°
Nuvasive, Inc.
6771307
In Commercial Distribution

  • 00887517809933 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809919

Interlock II, 12x17x14mm 30°
Nuvasive, Inc.
6771230
In Commercial Distribution

  • 00887517809919 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809896

Interlock II, 12x17x14mm 25°
Nuvasive, Inc.
6771225
In Commercial Distribution

  • 00887517809896 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809872

Interlock II, 12x17x14mm 20°
Nuvasive, Inc.
6771220
In Commercial Distribution

  • 00887517809872 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809858

Interlock II, 12x17x14mm 15°
Nuvasive, Inc.
6771215
In Commercial Distribution

  • 00887517809858 ()


  • Polymeric spinal interbody fusion cage
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