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.

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