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, 16x13x40mm 4°
Nuvasive, Inc.
5163404
In Commercial Distribution

  • 00887517575821 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x13x40mm 0°
Nuvasive, Inc.
5163400
In Commercial Distribution

  • 00887517575814 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x13x36mm 8°
Nuvasive, Inc.
5163368
In Commercial Distribution

  • 00887517575807 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x13x36mm 4°
Nuvasive, Inc.
5163364
In Commercial Distribution

  • 00887517575791 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x13x36mm 0°
Nuvasive, Inc.
5163360
In Commercial Distribution

  • 00887517575784 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x12x40mm 8°
Nuvasive, Inc.
5162408
In Commercial Distribution

  • 00887517575777 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x12x40mm 4°
Nuvasive, Inc.
5162404
In Commercial Distribution

  • 00887517575760 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x12x40mm 0°
Nuvasive, Inc.
5162400
In Commercial Distribution

  • 00887517575753 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x12x36mm 8°
Nuvasive, Inc.
5162368
In Commercial Distribution

  • 00887517575746 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 16x12x36mm 4°
Nuvasive, Inc.
5162364
In Commercial Distribution

  • 00887517575739 ()


  • Polymeric spinal interbody fusion cage
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