Stryker OrthoMap Versatile Hip System

Stryker OrthoMap Versatile Hip System is an FDA 510(k)-cleared medical device (K162937) 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 February 22, 2017. Regulation: 8.