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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 - 00887517823939

Interlock II Trial, 16x19x16mm 20°
Nuvasive, Inc.
6777216
In Commercial Distribution

  • 00887517823939 ()


  • Spinal implant trial

CoRoent - 00887517823922

Interlock II Trial, 15x19x16mm 20°
Nuvasive, Inc.
6777215
In Commercial Distribution

  • 00887517823922 ()


  • Spinal implant trial

CoRoent - 00887517823915

Interlock II Trial, 14x19x16mm 20°
Nuvasive, Inc.
6777214
In Commercial Distribution

  • 00887517823915 ()


  • Spinal implant trial

CoRoent - 00887517823908

Interlock II Trial, 13x19x16mm 20°
Nuvasive, Inc.
6777213
In Commercial Distribution

  • 00887517823908 ()


  • Spinal implant trial

CoRoent - 00887517823892

Interlock II Trial, 12x19x16mm 20°
Nuvasive, Inc.
6777212
In Commercial Distribution

  • 00887517823892 ()


  • Spinal implant trial

CoRoent - 00887517823885

Interlock II Trial, 11x19x16mm 20°
Nuvasive, Inc.
6777211
In Commercial Distribution

  • 00887517823885 ()


  • Spinal implant trial

CoRoent - 00887517823878

Interlock II Trial, 10x19x16mm 20°
Nuvasive, Inc.
6777210
In Commercial Distribution

  • 00887517823878 ()


  • Spinal implant trial

CoRoent - 00887517823861

Interlock II Trial, 9x19x16mm 20°
Nuvasive, Inc.
6777209
In Commercial Distribution

  • 00887517823861 ()


  • Spinal implant trial

CoRoent - 00887517813664

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

  • 00887517813664 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517813602

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

  • 00887517813602 ()


  • Polymeric spinal interbody fusion cage
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