K-number	K241259
Device name	Amplatz Goose Neck Snare Kit
Applicant	Medtronic, Inc.
Product code	MMX
Device class	Class II
Decision date	Jun 3, 2024
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Amplatz Goose Neck Snare Kit

Everything you need for a 510(k) submission. Nothing you don't.