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 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.
