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.
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