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FDA 510(k)

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

K-Number: K173352 · 2018-02-15

ApplicantConcentric Medical, Inc.
Decision Date2018-02-15
Product CodePOL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

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.

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. 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.

Other records listing Concentric Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: POL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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