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 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.
