Scottsdale, AZ – November 11, 2024 – OrthoSpineNews – Foundation Surgical, an innovative leader in spinal implant technology, is thrilled to announce the US Food & Drug Administration (FDA) 510(k) clearance of its Vertiwedge® Intraosseous Device! This novel, motion-sparing partial vertebral body replacement device along with its Vertebral Body Osteotomy (VBO®) procedure is set to redefine the landscape of lateral and motion-sparing spinal procedures.