Analyst Research

Report Title Price
Provider: Reuters Investment Profile
$20.00

NYSE and AMEX quotes delayed by at least 20 minutes. NASDAQ delayed by at least 15 minutes. For a complete list of exchanges and delays, please click here.

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. 

Company Quote

6.0
-0.09 -1.48%
8:35am EST