Centric Medical received expanded FDA 510(k) clearance to market its Cannulated Screw Internal Fixation System in foot/ankle reconstruction.
New options for the line, which received its first 510(k) clearance in 2015, include indications specifically for the forefoot in 2.0, 2.5 and 3.0mm diameters with headed and headless designs. The initial clearance addressed 0.5 to 7.5mm diameters indicated for midfoot and hindfoot, headed and headless.
Centric Medical received expanded FDA 510(k) clearance to market its Cannulated Screw Internal Fixation System in foot/ankle reconstruction.
New options for the line, which received its first 510(k) clearance in 2015, include indications specifically for the forefoot in 2.0, 2.5 and 3.0mm diameters with headed and headless designs. The initial...
Centric Medical received expanded FDA 510(k) clearance to market its Cannulated Screw Internal Fixation System in foot/ankle reconstruction.
New options for the line, which received its first 510(k) clearance in 2015, include indications specifically for the forefoot in 2.0, 2.5 and 3.0mm diameters with headed and headless designs. The initial clearance addressed 0.5 to 7.5mm diameters indicated for midfoot and hindfoot, headed and headless.
Copy to clipboard 
