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, 10x9x36mm 0°
Nuvasive, Inc.
5109360
In Commercial Distribution

  • 00887517573926 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x40mm 4°
Nuvasive, Inc.
5104404
In Commercial Distribution

  • 00887517573902 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x40mm 0°
Nuvasive, Inc.
5104400
In Commercial Distribution

  • 00887517573896 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x36mm 0°
Nuvasive, Inc.
5104360
In Commercial Distribution

  • 00887517573865 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x13x40mm 8°
Nuvasive, Inc.
5103408
In Commercial Distribution

  • 00887517573858 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x13x40mm 4°
Nuvasive, Inc.
5103404
In Commercial Distribution

  • 00887517573841 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x13x40mm 0°
Nuvasive, Inc.
5103400
In Commercial Distribution

  • 00887517573834 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x13x36mm 8°
Nuvasive, Inc.
5103368
In Commercial Distribution

  • 00887517573827 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x13x36mm 4°
Nuvasive, Inc.
5103364
In Commercial Distribution

  • 00887517573810 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x13x36mm 0°
Nuvasive, Inc.
5103360
In Commercial Distribution

  • 00887517573803 ()


  • Polymeric spinal interbody fusion cage
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