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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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Brigade - 00887517390691

CoRoent XLR-F, 14x42x30mm 8°
Nuvasive, Inc.
8921442
In Commercial Distribution

  • 00887517390691 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390684

CoRoent XLR-F, 14x38x28mm 8°
Nuvasive, Inc.
8921438
In Commercial Distribution

  • 00887517390684 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390677

CoRoent XLR-F, 14x34x24mm 8°
Nuvasive, Inc.
8921434
In Commercial Distribution

  • 00887517390677 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390660

CoRoent XLR-F, 12x42x30mm 8°
Nuvasive, Inc.
8921242
In Commercial Distribution

  • 00887517390660 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390653

CoRoent XLR-F, 12x38x28mm 8°
Nuvasive, Inc.
8921238
In Commercial Distribution

  • 00887517390653 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390646

CoRoent XLR-F, 12x34x24mm 8°
Nuvasive, Inc.
8921234
In Commercial Distribution

  • 00887517390646 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390639

CoRoent XLR-F, 10x42x30mm 8°
Nuvasive, Inc.
8921042
In Commercial Distribution

  • 00887517390639 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390622

CoRoent XLR-F, 10x38x28mm 8°
Nuvasive, Inc.
8921038
In Commercial Distribution

  • 00887517390622 ()


  • Polymeric spinal interbody fusion cage

Brigade - 00887517390615

CoRoent XLR-F, 10x34x24mm 8°
Nuvasive, Inc.
8921034
In Commercial Distribution

  • 00887517390615 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517390547

CoRoent® XL Wide, 10x22x60mm
Nuvasive, Inc.
6910260
In Commercial Distribution

  • 00887517390547 ()


  • Polymeric spinal interbody fusion cage
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