K-number	K082625
Device name	SYNTHES (USA) 3.5MM LCP PERIARTICULAR PROXIMAL HUMERUS PLATES
Applicant	Synthes (Usa)
Product code	HRS
Device class	Class II
Decision date	Dec 17, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SYNTHES (USA) 3.5MM LCP PERIARTICULAR PROXIMAL HUMERUS PLATES

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