Stryker Consolidated Operating Room Equipment (CORE) 2 Console

Stryker Consolidated Operating Room Equipment (CORE) 2 Console is an FDA 510(k)-cleared medical device (K171840) manufactured by Stryker Corporation. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 14, 2017. Regulation: 8.