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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 Class Implantable

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CoRoent - 00887517613721

CoRoent XL-L+, 13x16x60mm 10°
Nuvasive, Inc.
6313660006
In Commercial Distribution

  • 00887517613721 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613714

CoRoent XL-L+, 13x16x55mm 10°
Nuvasive, Inc.
6313655006
In Commercial Distribution

  • 00887517613714 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613707

CoRoent XL-L+, 13x16x50mm 10°
Nuvasive, Inc.
6313650006
In Commercial Distribution

  • 00887517613707 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613691

CoRoent XL-L+, 13x16x45mm 10°
Nuvasive, Inc.
6313645006
In Commercial Distribution

  • 00887517613691 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613684

CoRoent XL-L+, 13x16x40mm 10°
Nuvasive, Inc.
6313640006
In Commercial Distribution

  • 00887517613684 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613660

CoRoent XL-L+, 12x16x60mm 10°
Nuvasive, Inc.
6312660006
In Commercial Distribution

  • 00887517613660 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613653

CoRoent XL-L+, 12x16x55mm 10°
Nuvasive, Inc.
6312655006
In Commercial Distribution

  • 00887517613653 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613646

CoRoent XL-L+, 12x16x50mm 10°
Nuvasive, Inc.
6312650006
In Commercial Distribution

  • 00887517613646 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613639

CoRoent XL-L+, 12x16x45mm 10°
Nuvasive, Inc.
6312645006
In Commercial Distribution

  • 00887517613639 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517613622

CoRoent XL-L+, 12x16x40mm 10°
Nuvasive, Inc.
6312640006
In Commercial Distribution

  • 00887517613622 ()


  • Polymeric spinal interbody fusion cage
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