K-number	K090880
Device name	XYLOS POROUS SURGICAL MESH
Applicant	Xylos Corporation
Product code	FTM
Device class	Class II
Decision date	May 27, 2009
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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XYLOS POROUS SURGICAL MESH

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