Device typePolymeric 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 in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] 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 included with the device.
FDA categoryIntervertebral Fusion Device With Bone Graft, Lumbar
Device ID90814008024608
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information
Length29 Millimeter
Width39 Millimeter
Height12 Millimeter
Angle12 degree
Size29x39 12mm 12 degree