K-number	K181001
Device name	Medtronic Confida Brecker Guidewire
Applicant	Medtronic Core Valve, LLC
Product code	DQX
Device class	Class II
Decision date	May 3, 2018
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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Medtronic Confida Brecker Guidewire

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