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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 - 00887517823120

Interlock II Trial, 13x17x14mm 20°
Nuvasive, Inc.
6774213
In Commercial Distribution

  • 00887517823120 ()


  • Spinal implant trial

CoRoent - 00887517823113

Interlock II Trial, 12x17x14mm 20°
Nuvasive, Inc.
6774212
In Commercial Distribution

  • 00887517823113 ()


  • Spinal implant trial

CoRoent - 00887517823106

Interlock II Trial, 11x17x14mm 20°
Nuvasive, Inc.
6774211
In Commercial Distribution

  • 00887517823106 ()


  • Spinal implant trial

CoRoent - 00887517823090

Interlock II Trial, 10x17x14mm 20°
Nuvasive, Inc.
6774210
In Commercial Distribution

  • 00887517823090 ()


  • Spinal implant trial

CoRoent - 00887517823083

Interlock II Trial, 9x17x14mm 20°
Nuvasive, Inc.
6774209
In Commercial Distribution

  • 00887517823083 ()


  • Spinal implant trial

CoRoent - 00887517823076

Interlock II Trial, 8x17x14mm 20°
Nuvasive, Inc.
6774208
In Commercial Distribution

  • 00887517823076 ()


  • Spinal implant trial

CoRoent - 00887517812841

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

  • 00887517812841 ()


  • 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 - 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
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