Trevo XP ProVue Retriever and Trevo NXT™ ProVue Retriever

Trevo XP ProVue Retriever and Trevo NXT™ ProVue Retriever is an FDA 510(k)-cleared medical device (K203219) manufactured by Stryker Neurovascular. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 28, 2020. Regulation: 8.