1. SurGenTec has earned FDA clearance for its proprietary TiLink-L Sacroiliac Joint Fusion System, which can be implanted from a lateral or posterior/oblique approach and uses unique surface technology to optimize bone growth.
2. Icotec’s Vader pedicle system navigated instruments earned FDA 510(k) clearance.
3. Curiteva received FDA 510(k) approval for its pedicle and sacroiliac joint navigation instruments.
4. ZimVie earned FDA approval for its new version of the Mobi-C cervical disc.
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.
