SpinePoint earned the FDA’s 510(k) clearance for its Flex-Z cervical cage, according to a March 27 news release shared with Becker’s.
The Flex-Z cage is designed to address stiffness mismatches between conventional interbody implants and vertebral bone. It’s made with a 3D-printed porous titanium architecture and a patented Z shape for cushioning.
It’s the first cleared product in a larger platform of eight interbody devices.
SpinePoint is founded by Lali Sekhon, MD, PhD.
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.
