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, Cervical
Device ID90814008024196
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information
Length12 Millimeter
Width14 Millimeter
Height7 Millimeter
Angle6 degree
Size12X14 7mm 6 degree