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FDA 510(k)

TREVO RETRIEVER

K-Number: K120961 · 2012-08-03

ApplicantConcentric Medical, Inc.
Decision Date2012-08-03
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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 2012-08-03 under 510(k) number K120961. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREVO RETRIEVER?

TREVO RETRIEVER is a medical device that received FDA 510(k) clearance on 2012-08-03. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K120961.

When did TREVO RETRIEVER receive FDA 510(k) clearance?

TREVO RETRIEVER received FDA 510(k) clearance on 2012-08-03, under 510(k) number K120961.

Who is the listed applicant for 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 RETRIEVER?

The FDA product code for TREVO RETRIEVER is NRY.

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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.

K173352Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)K131437MODIFIED CONCENTRIC MICROCATHETERK131492MODIFIED FLOWGATE BALLOON GUIDE CATHETERK122581MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254K122478MODIFIED TREVO RETRIEVERK112404CONCENTRIC BALLOON GUIDE CATHETER

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Related Devices (Code: NRY)

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.

K261089Radical 064 Reperfusion Catheter; Radical 076 Reperfusion Catheter; Radical Aspiration Tubing KitMaduro Medical, Inc.K260617Tigertriever 13 Ultra Revascularization DeviceRapid Medical Ltd.K262398CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing setCERENOVUS, Inc.K262399Millipede SystemPerfuze, Ltd.K262391APRO 35 Swift Catheter and Alembic Aspiration TubingAlembic, LLCK260002Socrates Aspiration System (Socrates 70 Aspiration Catheter)Scientia Vascular, Inc.

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.

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