Mako Total Hip Application, Mako Total Knee Application

Mako Total Hip Application, Mako Total Knee Application is an FDA 510(k)-cleared medical device (K191998) manufactured by Mako Surgical Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 23, 2019. Regulation: 8.