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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 - 00887517310927

CoRoent® XLW Ti, 8x22x50mm 10°
Nuvasive, Inc.
6420850
In Commercial Distribution

  • 00887517310927 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310910

CoRoent® XLW Ti, 8x22x45mm 10°
Nuvasive, Inc.
6420845
In Commercial Distribution

  • 00887517310910 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310903

CoRoent® XLW Ti, 8x22x40mm 10°
Nuvasive, Inc.
6420840
In Commercial Distribution

  • 00887517310903 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310590

CoRoent® XLW Ti, 16x22x60mm
Nuvasive, Inc.
6416260
In Commercial Distribution

  • 00887517310590 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310583

CoRoent XLW Ti, 16x22x55mm
Nuvasive, Inc.
6416255
In Commercial Distribution

  • 00887517310583 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310576

CoRoent® XLW Ti, 16x22x50mm
Nuvasive, Inc.
6416250
In Commercial Distribution

  • 00887517310576 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310569

CoRoent XLW Ti, 16x22x45mm
Nuvasive, Inc.
6416245
In Commercial Distribution

  • 00887517310569 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310552

CoRoent XLW Ti, 16x22x40mm
Nuvasive, Inc.
6416240
In Commercial Distribution

  • 00887517310552 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310545

CoRoent® XLW Ti, 14x22x60mm
Nuvasive, Inc.
6414260
In Commercial Distribution

  • 00887517310545 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310538

CoRoent® XLW Ti, 14x22x55mm
Nuvasive, Inc.
6414255
In Commercial Distribution

  • 00887517310538 ()


  • Polymeric spinal interbody fusion cage
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