K-number	K082828
Device name	SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE
Applicant	Suturtek Incorporated
Product code	GAQ
Device class	Class II
Decision date	Oct 14, 2008
Decision	Substantially Equivalent
Regulation	878.4495

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View the full FDA submission: accessdata.fda.gov

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SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE

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