Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm

DEN150049 is the FDA 510(k) clearance record for Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mm, a class II device, cleared for Concentric Medical, Inc. on 2016-09-02 under FDA product code POL (Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment). FDA's definition for product code POL reads: "A neurovascular mechanical thrombectomy device for acute ischemic stroke treatment is a prescription device used in the treatment of acute ischemic stroke to improve clinical outcomes. The device is delivered into the neurovasculature with...". FDA records list 46 510(k) clearances for Concentric Medical, Inc., from 2001-03-07 to 2018-02-15. As of 2026-09-10, FDA records show no recalls naming DEN150049.