K-number	K061030
Device name	BIOBLANKET SURGICAL MESH
Applicant	Kensey Nash Corporation
Product code	FTM
Device class	Class II
Decision date	May 9, 2006
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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BIOBLANKET SURGICAL MESH

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