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 Class Implantable

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CoRoent Ant TLIF Ti, 9x10x32mm 4°
Nuvasive, Inc.
5290324
In Commercial Distribution

  • 00887517579478 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x10x32mm 0°
Nuvasive, Inc.
5290320
In Commercial Distribution

  • 00887517579461 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x14x32mm 8°
Nuvasive, Inc.
5284328
In Commercial Distribution

  • 00887517579454 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x14x32mm 4°
Nuvasive, Inc.
5284324
In Commercial Distribution

  • 00887517579447 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x14x32mm 0°
Nuvasive, Inc.
5284320
In Commercial Distribution

  • 00887517579430 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x13x32mm 8°
Nuvasive, Inc.
5283328
In Commercial Distribution

  • 00887517579423 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x13x32mm 4°
Nuvasive, Inc.
5283324
In Commercial Distribution

  • 00887517579416 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x13x32mm 0°
Nuvasive, Inc.
5283320
In Commercial Distribution

  • 00887517579409 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x12x32mm 8°
Nuvasive, Inc.
5282328
In Commercial Distribution

  • 00887517579393 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 8x12x32mm 4°
Nuvasive, Inc.
5282324
In Commercial Distribution

  • 00887517579386 ()


  • Polymeric spinal interbody fusion cage
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