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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 - 00887517310163

CoRoent® XLW Ti, 12x22x45mm
Nuvasive, Inc.
6412245
In Commercial Distribution

  • 00887517310163 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310156

CoRoent® XLW Ti, 12x22x40mm
Nuvasive, Inc.
6412240
In Commercial Distribution

  • 00887517310156 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310149

CoRoent® XLW Ti, 10x22x60mm
Nuvasive, Inc.
6410260
In Commercial Distribution

  • 00887517310149 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310132

CoRoent® XLW Ti, 10x22x55mm
Nuvasive, Inc.
6410255
In Commercial Distribution

  • 00887517310132 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310125

CoRoent® XLW Ti, 10x22x50mm
Nuvasive, Inc.
6410250
In Commercial Distribution

  • 00887517310125 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310118

CoRoent® XLW Ti, 10x22x45mm
Nuvasive, Inc.
6410245
In Commercial Distribution

  • 00887517310118 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517310101

CoRoent® XLW Ti, 10x22x40mm
Nuvasive, Inc.
6410240
In Commercial Distribution

  • 00887517310101 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517309792

CoRoent® XLW Ti, 8x22x60mm
Nuvasive, Inc.
6408260
In Commercial Distribution

  • 00887517309792 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517309785

CoRoent® XLW Ti, 8x22x55mm
Nuvasive, Inc.
6408255
In Commercial Distribution

  • 00887517309785 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517309778

CoRoent® XLW Ti, 8x22x50mm
Nuvasive, Inc.
6408250
In Commercial Distribution

  • 00887517309778 ()


  • Polymeric spinal interbody fusion cage
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