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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 - 00887517303622

CoRoent® XL-H, 2x22x50mm 30°
Nuvasive, Inc.
6300250
In Commercial Distribution

  • 00887517303622 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517303615

CoRoent® XL-H, 2x22x45mm 30°
Nuvasive, Inc.
6300245
In Commercial Distribution

  • 00887517303615 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300911

CoRoent® XLK, 18x18x60mm 10°
Nuvasive, Inc.
6221860
In Commercial Distribution

  • 00887517300911 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300904

CoRoent® XLK, 18x18x55mm 10°
Nuvasive, Inc.
6221855
In Commercial Distribution

  • 00887517300904 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300591

CoRoent® XLK, 18x18x50mm 10°
Nuvasive, Inc.
6221850
In Commercial Distribution

  • 00887517300591 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300584

CoRoent® XLK, 18x18x45mm 10°
Nuvasive, Inc.
6221845
In Commercial Distribution

  • 00887517300584 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300577

CoRoent® XLK, 16x18x60mm 10°
Nuvasive, Inc.
6221660
In Commercial Distribution

  • 00887517300577 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300560

CoRoent® XLK, 16x18x55mm 10°
Nuvasive, Inc.
6221655
In Commercial Distribution

  • 00887517300560 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300553

CoRoent® XLK, 16x18x50mm 10°
Nuvasive, Inc.
6221650
In Commercial Distribution

  • 00887517300553 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517300546

CoRoent® XLK, 16x18x45mm 10°
Nuvasive, Inc.
6221645
In Commercial Distribution

  • 00887517300546 ()


  • Polymeric spinal interbody fusion cage
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