Trevo NXT ProVue Retriever

Trevo NXT ProVue Retriever is an FDA 510(k)-cleared medical device (K210502) 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 August 26, 2021. Regulation: 8.