K-number	K113523
Device name	LIMACORPORATE SMR REVERSE SHOULDER SYSTEM
Applicant	Lima Corporate S.P.A.
Product code	PHX
Device class	Class II
Decision date	Dec 20, 2011
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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LIMACORPORATE SMR REVERSE SHOULDER SYSTEM

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