K-number	K162752
Device name	ARTIA Reconstructive Tissue Matrix Perforated
Applicant	Lifecell Corporation
Product code	FTM
Device class	Class II
Decision date	Feb 24, 2017
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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ARTIA Reconstructive Tissue Matrix Perforated

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