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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 - 00887517389701

CoRoent® XL, 8x18x50mm
Nuvasive, Inc.
6908850
In Commercial Distribution

  • 00887517389701 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517389497

CoRoent® XL, 8x18x45mm
Nuvasive, Inc.
6908845
In Commercial Distribution

  • 00887517389497 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517389480

CoRoent® XL, 8x18x40mm
Nuvasive, Inc.
6908840
In Commercial Distribution

  • 00887517389480 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517389473

CoRoent® XL Wide, 8x22x60mm
Nuvasive, Inc.
6908260
In Commercial Distribution

  • 00887517389473 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517389466

CoRoent® XL Wide, 8x22x55mm
Nuvasive, Inc.
6908255
In Commercial Distribution

  • 00887517389466 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517389459

CoRoent® XL Wide, 8x22x50mm
Nuvasive, Inc.
6908250
In Commercial Distribution

  • 00887517389459 ()


  • Polymeric spinal interbody fusion cage

NuVasive - 00887517389091

Universal Inserter, XLIF Angled
Nuvasive, Inc.
6904485
In Commercial Distribution

  • 00887517389091 ()


  • Orthopaedic implant inserter/extractor, reusable

NuVasive - 00887517388209

Universal Trial 12x22x60mm CoRoent XLW
Nuvasive, Inc.
6901612
In Commercial Distribution

  • 00887517388209 ()


  • Spinal implant trial

NuVasive - 00887517387899

Universal Trial 10x22x60mm CoRoent XLW
Nuvasive, Inc.
6901610
In Commercial Distribution

  • 00887517387899 ()


  • Spinal implant trial

NuVasive - 00887517387882

Universal Trial 8x22x60mm CoRoent XLW
Nuvasive, Inc.
6901608
In Commercial Distribution

  • 00887517387882 ()


  • Spinal implant trial
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