FloSpine earns FDA clearance for KeyLift system

FloSpine earned FDA 510(k) clearance for its KeyLift expandable interlaminar stabilization system, according to a Nov. 1 news release.

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The device addresses spinal stenosis and is designed to be a less invasive alternative. It can expand up to 4mm in hight and promotes disc health by balancing the intervertebral discs. 

“As a spine surgeon of over 25 years, I believe this technology will reach more patients by enabling more interventional physicians to treat mild to moderate spinal stenosis without the fear of a large surgery,” Cheng-Lun Soo, MD, co-inventor of the device, said in the release.

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.

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