K-number	K130400
Device name	MERETEC CS, CORTICAL SCREWS
Applicant	Merete Medical GmbH
Product code	HWC
Device class	Class II
Decision date	Apr 5, 2013
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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MERETEC CS, CORTICAL SCREWS

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