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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 - 00887517809551

Interlock II, 9x17x14mm 20°
Nuvasive, Inc.
6770920
In Commercial Distribution

  • 00887517809551 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809476

Interlock II, 8x17x14mm 20°
Nuvasive, Inc.
6770820
In Commercial Distribution

  • 00887517809476 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811394

Interlock II, 12x19x16mm 20°
Nuvasive, Inc.
6779220
In Commercial Distribution

  • 00887517811394 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811295

Interlock II, 11x19x16mm 20°
Nuvasive, Inc.
6779120
In Commercial Distribution

  • 00887517811295 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811196

Interlock II, 10x19x16mm 20°
Nuvasive, Inc.
6779020
In Commercial Distribution

  • 00887517811196 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811110

Interlock II, 9x19x16mm 20°
Nuvasive, Inc.
6778920
In Commercial Distribution

  • 00887517811110 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811639

Interlock II, 14x19x16mm 20°
Nuvasive, Inc.
6779420
In Commercial Distribution

  • 00887517811639 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811516

Interlock II, 13x19x16mm 20°
Nuvasive, Inc.
6779320
In Commercial Distribution

  • 00887517811516 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811875

Interlock II, 16x19x16mm 20°
Nuvasive, Inc.
6779620
In Commercial Distribution

  • 00887517811875 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517811752

Interlock II, 15x19x16mm 20°
Nuvasive, Inc.
6779520
In Commercial Distribution

  • 00887517811752 ()


  • Polymeric spinal interbody fusion cage
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