K-number	K113084
Device name	RENOVIS CANNULATED SCREW SYSTEM
Applicant	Renovis Surgical Technologies, LLC
Product code	HWC
Device class	Class II
Decision date	Dec 9, 2011
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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RENOVIS CANNULATED SCREW SYSTEM

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