1. Eminent Spine, a biomechanical provider, has earned approval from the U.S. Food and Drug Administration for its 3D-printed titanium cervical intervertebral body fusion device system.
2. NuVasive’s Modulus cervical interbody implant was approved by the FDA for use with a bone void filler.
3. FloSpine’s 3D-printed Ti-Largo earned FDA 510(k) clearance. The titanium cage is designed for cervical spine procedures and has a highly porous surface.
5. Aurora Spine earned Institutional Review Board approval to begin a multicenter study of its Dexa-C cervical interbody system.
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.
