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, Intervertebral Fusion Device With Integrated Fixation, Cervical
Device IDB806ISRO1620L07CA10
Catalog numberISRO1620L07CA1
AvailabilityPrescription
Single useYes
SterileYes
LatexNot made with natural rubber latex
MRI safetyLabeling does not contain MRI Safety Information
Depth16 Millimeter
Angle6 degree
Width20 Millimeter
Height07 Millimeter