K-number	K220305
Device name	Syntheon LAA Exclusion System, Syntheon LAA Selection Guide
Applicant	Syntheon
Product code	PZX
Device class	Class II
Decision date	Oct 28, 2022
Decision	Substantially Equivalent
Regulation	878.4300

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Source

View the full FDA submission: accessdata.fda.gov

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Syntheon LAA Exclusion System, Syntheon LAA Selection Guide

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