Stryker MIS and Footed Attachments

Stryker MIS and Footed Attachments is an FDA 510(k)-cleared medical device (K191049) manufactured by Stryker Corporation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 17, 2019. Regulation: 8.