Device typeMetallic spinal interbody fusion cage: A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated cylindrical, or disc-shaped device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.
FDA categorySPINAL VERTEBRAL BODY REPLACEMENT DEVICE
Device ID00191375000013
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information
Width32 Millimeter
Depth21 Millimeter
Sizewidth(MLxAP), 32 x 21, mm
Angle7 degree
Height20 Millimeter
SizeLordotic Angle 7 Deg