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 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.
