K-number	K073523
Device name	INTERCEPTOR PLUS CORONARY FILTER SYSTEMS
Applicant	Medtronic, Inc.
Product code	NFA
Device class	Class II
Decision date	Aug 1, 2008
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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INTERCEPTOR PLUS CORONARY FILTER SYSTEMS

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