FDA 510(k)

Amplatz Goose Neck Snare Kit

K-Number: K241259 · 2024-06-03

Decision Date2024-06-03

Product CodeMMX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Amplatz Goose Neck Snare Kit is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2024-06-03 under 510(k) number K241259. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Amplatz Goose Neck Snare Kit?

Amplatz Goose Neck Snare Kit is a medical device that received FDA 510(k) clearance on 2024-06-03. The listed applicant is Medtronic, Inc.. The 510(k) number is K241259.

When did Amplatz Goose Neck Snare Kit receive FDA 510(k) clearance?

Amplatz Goose Neck Snare Kit received FDA 510(k) clearance on 2024-06-03, under 510(k) number K241259.

Who is the listed applicant for Amplatz Goose Neck Snare Kit?

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

What is the FDA product code for Amplatz Goose Neck Snare Kit?

The FDA product code for Amplatz Goose Neck Snare Kit is MMX.

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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.