K-number	K132025
Device name	MESO BILAYER SURGICAL MESH
Applicant	Kensey Nash Corporation Dba Dsm Biomedical
Product code	FTM
Device class	Class II
Decision date	Oct 30, 2013
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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MESO BILAYER SURGICAL MESH

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