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Spineguard SA Receives FDA 510(k) Clearance for Miniaturized and Directional Versions of Its PediGuard Platform

Wednesday, 28 Aug 2013 11:40am EDT 

Spineguard SA announced that it has received FDA 510(k) clearance of three new products that complete its PediGuard platform of single-use drilling instruments which secure the pedicle screw pilot hole: two miniaturized versions of its classic and curved range, and a directional version of its cannulated series. PediGuard is a handheld device capable of alerting surgeons to potential pedicular or vertebral breaches. Real-time feedback is provided via audio and visual signals. 

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