FDA 510(k)

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

Número K: K173352 · 2018-02-15

Data da decisão2018-02-15

Código do produtoPOL

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) is the device name listed in this FDA 510(k) record. The listed applicant is Concentric Medical, Inc.. It received FDA 510(k) clearance on 2018-02-15 under 510(k) number K173352. The device is classified under product code POL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

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. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K173352.

When did Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) receive FDA 510(k) clearance?

Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever) received FDA 510(k) clearance on 2018-02-15, under 510(k) number K173352.

Who is the listed applicant for Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)?

The FDA 510(k) record lists Concentric Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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