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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 - 00887517322784

CoRoent XL Ti, 11x18x45mm 10°
Nuvasive, Inc.
6481145
In Commercial Distribution

  • 00887517322784 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322777

CoRoent XL Ti, 11x18x40mm 10°
Nuvasive, Inc.
6481140
In Commercial Distribution

  • 00887517322777 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322760

CoRoent XL Ti, 9x18x60mm 10°
Nuvasive, Inc.
6480960
In Commercial Distribution

  • 00887517322760 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322753

CoRoent XL Ti, 9x18x55mm 10°
Nuvasive, Inc.
6480955
In Commercial Distribution

  • 00887517322753 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322746

CoRoent XL Ti, 9x18x50mm 10°
Nuvasive, Inc.
6480950
In Commercial Distribution

  • 00887517322746 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322739

CoRoent XL Ti, 9x18x45mm 10°
Nuvasive, Inc.
6480945
In Commercial Distribution

  • 00887517322739 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322722

CoRoent XL Ti, 9x18x40mm 10°
Nuvasive, Inc.
6480940
In Commercial Distribution

  • 00887517322722 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322715

CoRoent XLW Ti, 15x22x60mm 10°
Nuvasive, Inc.
6421560
In Commercial Distribution

  • 00887517322715 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322708

CoRoent XLW Ti, 15x22x55mm 10°
Nuvasive, Inc.
6421555
In Commercial Distribution

  • 00887517322708 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517322395

CoRoent XLW Ti, 15x22x50mm 10°
Nuvasive, Inc.
6421550
In Commercial Distribution

  • 00887517322395 ()


  • Polymeric spinal interbody fusion cage
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