K-number	K120854
Device name	SYNTHES VA LCP ANKLE TRAUMA SYSTEM
Applicant	Synthes USA
Product code	HRS
Device class	Class II
Decision date	Jun 18, 2012
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SYNTHES VA LCP ANKLE TRAUMA SYSTEM

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