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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 - 00887517810359

Interlock II, 16x17x14mm 20°
Nuvasive, Inc.
6771620
In Commercial Distribution

  • 00887517810359 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517810236

Interlock II, 15x17x14mm 20°
Nuvasive, Inc.
6771520
In Commercial Distribution

  • 00887517810236 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517810113

Interlock II, 14x17x14mm 20°
Nuvasive, Inc.
6771420
In Commercial Distribution

  • 00887517810113 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809995

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

  • 00887517809995 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809872

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

  • 00887517809872 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809759

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

  • 00887517809759 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517809650

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

  • 00887517809650 ()


  • Polymeric spinal interbody fusion cage

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 - 00887517681065

CoRoent XL-H, 10x22x60mm 20°
Nuvasive, Inc.
6201060P2
In Commercial Distribution

  • 00887517681065 ()


  • Polymeric spinal interbody fusion cage
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