K-number	K141084
Device name	Matristem Surgery Matrix RS, PSM, PSMX, Matristem Pelvic Floor Matrix
Applicant	Acell, Inc.
Product code	FTM
Device class	Class II
Decision date	Jun 17, 2015
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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Matristem Surgery Matrix RS, PSM, PSMX, Matristem Pelvic Floor Matrix

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