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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 - 00887517737229

CoRoent LO Ti, 16x10x35mm 5°
Nuvasive, Inc.
6081635P2
In Commercial Distribution

  • 00887517737229 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737212

CoRoent LO Ti, 16x10x30mm 5°
Nuvasive, Inc.
6081630P2
In Commercial Distribution

  • 00887517737212 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737205

CoRoent LO Ti, 16x10x25mm 5°
Nuvasive, Inc.
6081625P2
In Commercial Distribution

  • 00887517737205 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737199

CoRoent LO Ti, 15x10x40mm 5°
Nuvasive, Inc.
6081540P2
In Commercial Distribution

  • 00887517737199 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737182

CoRoent LO Ti, 15x10x35mm 5°
Nuvasive, Inc.
6081535P2
In Commercial Distribution

  • 00887517737182 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737175

CoRoent LO Ti, 15x10x30mm 5°
Nuvasive, Inc.
6081530P2
In Commercial Distribution

  • 00887517737175 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737168

CoRoent LO Ti, 15x10x25mm 5°
Nuvasive, Inc.
6081525P2
In Commercial Distribution

  • 00887517737168 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737151

CoRoent LO Ti, 13x10x40mm 5°
Nuvasive, Inc.
6081340P2
In Commercial Distribution

  • 00887517737151 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737144

CoRoent LO Ti, 13x10x35mm 5°
Nuvasive, Inc.
6081335P2
In Commercial Distribution

  • 00887517737144 ()


  • Polymeric spinal interbody fusion cage

CoRoent - 00887517737137

CoRoent LO Ti, 13x10x30mm 5°
Nuvasive, Inc.
6081330P2
In Commercial Distribution

  • 00887517737137 ()


  • Polymeric spinal interbody fusion cage
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