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 Ant TLIF Ti, 11x10x30mm 4°
Nuvasive, Inc.
5210304
In Commercial Distribution

  • 00887517569103 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 11x10x30mm 0°
Nuvasive, Inc.
5210300
In Commercial Distribution

  • 00887517569097 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 11x10x28mm 8°
Nuvasive, Inc.
5210288
In Commercial Distribution

  • 00887517569080 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 11x10x28mm 4°
Nuvasive, Inc.
5210284
In Commercial Distribution

  • 00887517569073 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 11x10x28mm 0°
Nuvasive, Inc.
5210280
In Commercial Distribution

  • 00887517569066 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x34mm 8°
Nuvasive, Inc.
5209348
In Commercial Distribution

  • 00887517569059 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x34mm 4°
Nuvasive, Inc.
5209344
In Commercial Distribution

  • 00887517569042 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x34mm 0°
Nuvasive, Inc.
5209340
In Commercial Distribution

  • 00887517569035 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x32mm 8°
Nuvasive, Inc.
5209328
In Commercial Distribution

  • 00887517569028 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x32mm 4°
Nuvasive, Inc.
5209324
In Commercial Distribution

  • 00887517569011 ()


  • Polymeric spinal interbody fusion cage
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