K-number	K073412
Device name	GRYPHON BR AND HEALIX BR ANCHORS
Applicant	Depuy Mitek, A Johnson & Johnson Company
Product code	MAI
Device class	Class II
Decision date	Jan 17, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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GRYPHON BR AND HEALIX BR ANCHORS

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