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FDA 510(k)

MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6

K-Number: K063774 · 2007-01-24

ApplicantConcentric Medical, Inc.
Decision Date2007-01-24
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6 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 2007-01-24 under 510(k) number K063774. 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 MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6?

MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6 is a medical device that received FDA 510(k) clearance on 2007-01-24. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K063774.

When did MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6 receive FDA 510(k) clearance?

MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6 received FDA 510(k) clearance on 2007-01-24, under 510(k) number K063774.

Who is the listed applicant for MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6?

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 MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6?

The FDA product code for MODIFICATION TO MERCI RETRIEVER, MODELS X5 AND X6 is NRY.

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Other records listing Concentric Medical, Inc. as applicant

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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.

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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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