K-number	K143392
Device name	Quattro Bolt Tenodesis Screw
Applicant	Cayenne Medical, Inc.
Product code	MBI
Device class	Class II
Decision date	Jan 23, 2015
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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Quattro Bolt Tenodesis Screw

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