Spineology Aquires FDA Clearance of Rampart Duo Interbody Fusion System
Spineology has received FDA clearance for the Rampart Duo Interbody Fusion system.
The device design includes PEEK spacer blocks that are positioned at each end of the device and a flexible porous graft containment mesh that creates a central graft cavity.
After implanting, the porous graft containment mesh is filled with bone graft to release the device in the anterior-posterior direction and in the superior-inferior direction to provide conforming apposition with the vertebral endplates.
“The implant design allows for decreased retraction requirements when compared to current interbody systems. The minimized tissue retraction may reduce the potential for nerve damage and resultant leg pain associated with the lateral approach,” the company said. — Cynthia Jessup