K-number	K992958
Device name	ADVANTA GRAFT (<6MM)
Applicant	Atrium Medical Corp.
Product code	DYF
Device class	Class II
Decision date	Oct 1, 1999
Decision	Substantially Equivalent
Regulation	870.3450

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View the full FDA submission: accessdata.fda.gov

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ADVANTA GRAFT (<6MM)

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