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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 - 00887517809834

Interlock II, 12x17x14mm 10°
Nuvasive, Inc.
6771210
In Commercial Distribution

  • 00887517809834 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809810

Interlock II, 12x17x14mm 7°
Nuvasive, Inc.
6771207
In Commercial Distribution

  • 00887517809810 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809797

Interlock II, 11x17x14mm 30°
Nuvasive, Inc.
6771130
In Commercial Distribution

  • 00887517809797 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809773

Interlock II, 11x17x14mm 25°
Nuvasive, Inc.
6771125
In Commercial Distribution

  • 00887517809773 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809759

Interlock II, 11x17x14mm 20°
Nuvasive, Inc.
6771120
In Commercial Distribution

  • 00887517809759 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809735

Interlock II, 11x17x14mm 15°
Nuvasive, Inc.
6771115
In Commercial Distribution

  • 00887517809735 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809711

Interlock II, 11x17x14mm 10°
Nuvasive, Inc.
6771110
In Commercial Distribution

  • 00887517809711 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809698

Interlock II, 11x17x14mm 7°
Nuvasive, Inc.
6771107
In Commercial Distribution

  • 00887517809698 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809674

Interlock II, 10x17x14mm 25°
Nuvasive, Inc.
6771025
In Commercial Distribution

  • 00887517809674 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809650

Interlock II, 10x17x14mm 20°
Nuvasive, Inc.
6771020
In Commercial Distribution

  • 00887517809650 ()


  • Polymeric spinal interbody fusion cage
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