Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)

Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) is an FDA 510(k)-cleared medical device (K173352) manufactured by Concentric Medical, Inc.. 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 14, 2018. Regulation: 8.