K-number	K020528
Device name	INTRASTENT LD (LARGE DIAMETER) STENT
Applicant	Sulzer Intratherapeutics, Inc.
Product code	FGE
Device class	Class II
Decision date	Apr 16, 2002
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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INTRASTENT LD (LARGE DIAMETER) STENT

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