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, 9x9x32mm 0°
Nuvasive, Inc.
5299320
In Commercial Distribution

  • 00887517573568 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x30mm 8°
Nuvasive, Inc.
5299308
In Commercial Distribution

  • 00887517573551 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x30mm 4°
Nuvasive, Inc.
5299304
In Commercial Distribution

  • 00887517573544 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x30mm 0°
Nuvasive, Inc.
5299300
In Commercial Distribution

  • 00887517573537 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x28mm 8°
Nuvasive, Inc.
5299288
In Commercial Distribution

  • 00887517573520 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x28mm 4°
Nuvasive, Inc.
5299284
In Commercial Distribution

  • 00887517573513 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x9x28mm 0°
Nuvasive, Inc.
5299280
In Commercial Distribution

  • 00887517573506 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x34mm 8°
Nuvasive, Inc.
5294348
In Commercial Distribution

  • 00887517573490 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x34mm 4°
Nuvasive, Inc.
5294344
In Commercial Distribution

  • 00887517573483 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x34mm 0°
Nuvasive, Inc.
5294340
In Commercial Distribution

  • 00887517573476 ()


  • Polymeric spinal interbody fusion cage
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