K-number	K993145
Device name	MEDTRONIC AVE BRIDGE STENT
Applicant	Medtronic Ave, Inc.
Product code	FGE
Device class	Class II
Decision date	Oct 21, 1999
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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MEDTRONIC AVE BRIDGE STENT

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