KLS Martin Individual Patient Solutions (IPS) Planning System

KLS Martin Individual Patient Solutions (IPS) Planning System is an FDA 510(k)-cleared medical device (K182889) manufactured by KLS-Martin L.P.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 25, 2019. Regulation: 8.