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Additive Orthopaedics receives FDA 510(k) clearance for bunion correction system

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Additive Orthopaedics LLC announced it has received FDA 510(k) clearance for its 3-D printed minimally invasive, intramedullary Bunion Correction System.

Designed to address alignment and stabilization of bunions, the Bunion Correction System is the company’s fourth 510(k) product clearance that leverages additive manufacturing and its sixth complete product line to receive 510(k) clearance, according to a company press release.

Reference:

http://www.additiveorthopaedics.com/home-1.html