K-number	K092207
Device name	RESTORELLE POLYPROPYLENE MESH
Applicant	Mpathy Medical Devices, Inc.
Product code	OTP
Device class	Class III
Decision date	Aug 4, 2009
Decision	Substantially Equivalent
Regulation	884.5980

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Source

View the full FDA submission: accessdata.fda.gov

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RESTORELLE POLYPROPYLENE MESH

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