1. Stryker earned 510(k) FDA clearance for its Q Guidance System with Cranial Guidance Software.
2. Alevio Spine received additional 510(k) clearance for the devicemaker’s SI-Cure sacroiliac joint fusion system.
3. The FDA extended its approval for Abbot’s Proclaim XR spinal cord stimulator.
4. Icotec’s Vader pedicle system to include 4.5 mm pedicle screws and extended carbon/PEEK rods received FDA clearance.
5. VySpine’s LumiVy NanoVy Ti lumbar interbody fusion system earned FDA clearance.
At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.
