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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 Size Device Class Implantable

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CoRoent - 00887517296269

CoRoent® XL-XW, 8x26x45mm
Nuvasive, Inc.
6208045
In Commercial Distribution

  • 00887517296269 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296221

CoRoent® XL-H, 10x22x60mm 20°
Nuvasive, Inc.
6201060
In Commercial Distribution

  • 00887517296221 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296214

CoRoent® XL-H, 10x22x55mm 20°
Nuvasive, Inc.
6201055
In Commercial Distribution

  • 00887517296214 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296207

CoRoent® XL-H, 10x22x50mm 20°
Nuvasive, Inc.
6201050
In Commercial Distribution

  • 00887517296207 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517295897

CoRoent® XL-H, 10x22x45mm 20°
Nuvasive, Inc.
6201045
In Commercial Distribution

  • 00887517295897 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517295873

CoRoent XLXW Inserter
Nuvasive, Inc.
6201000
In Commercial Distribution

  • 00887517295873 ()


  • Orthopaedic implant inserter/extractor, reusable

CoRoent - 00887517295859

CoRoent® XL-H, 8x22x60mm 20°
Nuvasive, Inc.
6200860
In Commercial Distribution

  • 00887517295859 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517295842

CoRoent® XL-H, 8x22x55mm 20°
Nuvasive, Inc.
6200855
In Commercial Distribution

  • 00887517295842 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517295835

CoRoent® XL-H, 8x22x50mm 20°
Nuvasive, Inc.
6200850
In Commercial Distribution

  • 00887517295835 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517295828

CoRoent® XL-H, 8x22x45mm 20°
Nuvasive, Inc.
6200845
In Commercial Distribution

  • 00887517295828 ()


  • Polymeric spinal interbody fusion cage
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