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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 Size Type Device Class Implantable

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CoRoent - 00887517297303

CoRoent® XL-XW, 10x26x60mm 10°
Nuvasive, Inc.
6210160
In Commercial Distribution

  • 00887517297303 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517297280

CoRoent® LO Ti, 8x10x25mm 10°
Nuvasive, Inc.
6090825
In Commercial Distribution

  • 00887517297280 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296986

CoRoent® XL-XW, 10x26x50mm 10°
Nuvasive, Inc.
6210150
In Commercial Distribution

  • 00887517296986 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296917

CoRoent® XL-XW, 10x26x50mm
Nuvasive, Inc.
6210050
In Commercial Distribution

  • 00887517296917 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296566

CoRoent® XL-XW, 8x26x60mm 10°
Nuvasive, Inc.
6208160
In Commercial Distribution

  • 00887517296566 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296535

CoRoent® XL-XW, 8x26x45mm 10°
Nuvasive, Inc.
6208145
In Commercial Distribution

  • 00887517296535 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296290

CoRoent® XL-XW, 8x26x60mm
Nuvasive, Inc.
6208060
In Commercial Distribution

  • 00887517296290 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517296283

CoRoent® XL-XW, 8x26x55mm
Nuvasive, Inc.
6208055
In Commercial Distribution

  • 00887517296283 ()


  • 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
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