
Synthes (Usa)
Free shipping on orders over $99 · 30-day returns
SYNTHES AIR PEN DRIVE (APD) SYSTEM is an FDA 510(k)-cleared medical device (K093361) manufactured by Synthes (Usa). This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 13, 2010. Regulation: 8.