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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, 14x14x30mm 0°
Nuvasive, Inc.
5244300P2
In Commercial Distribution

  • 00887517733337 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 14x11x30mm 0°
Nuvasive, Inc.
5241300P2
In Commercial Distribution

  • 00887517733306 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x9x30mm 0°
Nuvasive, Inc.
5229300P2
In Commercial Distribution

  • 00887517733276 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x14x30mm 0°
Nuvasive, Inc.
5224300P2
In Commercial Distribution

  • 00887517733252 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 12x11x30mm 0°
Nuvasive, Inc.
5221300P2
In Commercial Distribution

  • 00887517733221 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 11x9x30mm 0°
Nuvasive, Inc.
5219300P2
In Commercial Distribution

  • 00887517733191 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x9x30mm 0°
Nuvasive, Inc.
5209300P2
In Commercial Distribution

  • 00887517733139 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x14x30mm 0°
Nuvasive, Inc.
5204300P2
In Commercial Distribution

  • 00887517733115 ()


  • Polymeric spinal interbody fusion cage
CoRoent Ant TLIF Ti, 10x11x30mm 0°
Nuvasive, Inc.
5201300P2
In Commercial Distribution

  • 00887517733085 ()


  • Polymeric spinal interbody fusion cage
Duo Ti Angled Trial, 16mm, 0°
SPINEOLOGY INC.
86-11-21-16
In Commercial Distribution

  • M7408610041 ()
861-0041

  • Metallic spinal interbody fusion cage
  • Polymeric spinal interbody fusion cage
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