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, 9x9x32mm 8°
Nuvasive, Inc.
5299328
In Commercial Distribution

  • 00887517573582 ()


  • 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 4°
Nuvasive, Inc.
5299284
In Commercial Distribution

  • 00887517573513 ()


  • 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, 9x14x30mm 8°
Nuvasive, Inc.
5294308
In Commercial Distribution

  • 00887517573469 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x30mm 4°
Nuvasive, Inc.
5294304
In Commercial Distribution

  • 00887517573452 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x28mm 8°
Nuvasive, Inc.
5294288
In Commercial Distribution

  • 00887517573438 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x14x28mm 0°
Nuvasive, Inc.
5294280
In Commercial Distribution

  • 00887517573414 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 9x13x34mm 4°
Nuvasive, Inc.
5293344
In Commercial Distribution

  • 00887517573391 ()


  • Polymeric spinal interbody fusion cage
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