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FDA 510(k)

Amplatz Goose Neck Snare Kit

K-Number: K241259 · 2024-06-03

ApplicantMedtronic, Inc.
Decision Date2024-06-03
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Amplatz Goose Neck Snare Kit is a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2024-06-03 under approval 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. It is manufactured by Medtronic, Inc.. The 510(k) number is K241259.

When was Amplatz Goose Neck Snare Kit approved by the FDA?

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

What company makes Amplatz Goose Neck Snare Kit?

Amplatz Goose Neck Snare Kit is manufactured by Medtronic, Inc..

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.

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