K-number	K110110
Device name	ATRIUM CENTRILFX MESH
Applicant	Atrium Medical Corporation
Product code	FTL
Device class	Class II
Decision date	Feb 15, 2011
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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ATRIUM CENTRILFX MESH

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