Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
K-Number: K173352 · 2018-02-15
Device Summary
Frequently Asked Questions
What is the 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 a medical device that received FDA 510(k) clearance on 2018-02-15. It is manufactured by Concentric Medical, Inc.. The 510(k) number is K173352.
When was Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) approved by the FDA?
Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) received FDA 510(k) clearance on 2018-02-15, under approval number K173352.
What company makes 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 manufactured by Concentric Medical, Inc..
What is the FDA product code for Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)?
The FDA product code for Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) is POL.
Other Devices by Concentric Medical, Inc.
Related Devices (Code: POL)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.