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FDA 510(k)

AtriClip FLEX-Mini LAA Exclusion System (ACHM)

K-Number: K234125 · 2024-07-29

Decision Date2024-07-29
Product CodePZX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AtriClip FLEX-Mini LAA Exclusion System (ACHM) is a medical device manufactured by AtriCure, Inc.. It received FDA 510(k) clearance on 2024-07-29 under approval number K234125. The device is classified under product code PZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AtriClip FLEX-Mini LAA Exclusion System (ACHM)?

AtriClip FLEX-Mini LAA Exclusion System (ACHM) is a medical device that received FDA 510(k) clearance on 2024-07-29. It is manufactured by AtriCure, Inc.. The 510(k) number is K234125.

When was AtriClip FLEX-Mini LAA Exclusion System (ACHM) approved by the FDA?

AtriClip FLEX-Mini LAA Exclusion System (ACHM) received FDA 510(k) clearance on 2024-07-29, under approval number K234125.

What company makes AtriClip FLEX-Mini LAA Exclusion System (ACHM)?

AtriClip FLEX-Mini LAA Exclusion System (ACHM) is manufactured by AtriCure, Inc..

What is the FDA product code for AtriClip FLEX-Mini LAA Exclusion System (ACHM)?

The FDA product code for AtriClip FLEX-Mini LAA Exclusion System (ACHM) is PZX.

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Official Source

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