Spineguard SA: Business description, financial summary, 3yr and interim financials, key statistics/ratios and historical ratio analysis.
Provider: Reuters Investment Profile
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Spineguard SA Receives FDA 510(k) Clearance for Miniaturized and Directional Versions of Its PediGuard Platform
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.
Latest Developments for Spineguard SA
- Spineguard announces data on PediGuard device
- Spineguard SA Obtains Regulatory Clearance to Sell PediGuard Curved and Curved XS in Mexico
- Spineguard SA Receives Patents for Smart Screw in United States and China; Receives Regulatory Approvals in Mexico and Colombia
- Spineguard SA Receives Approval to Sell Its PediGuard Platform in Japan
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