K-number	K162934
Device name	Biodesign Parastomal Hernia Repair Graft
Applicant	Cook Biotech Incorporated
Product code	FTM
Device class	Class II
Decision date	Jul 10, 2017
Decision	Substantially Equivalent
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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Biodesign Parastomal Hernia Repair Graft

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