Aurora Spine sacroiliac joint fixation system receives FDA clearance

Spinal implant technology manufacturer Aurora Spine has received 510(k) clearance from the FDA for its new sacroiliac joint fixation system. 

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The SiLo TFX MIS sacroiliac joint fixation system is a minimally invasive system, according to an Oct. 4 news release from the company. 

Additional details about the device are expected to be disclosed by the company in the coming days.

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.

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