K-number	K153722
Device name	SMR 3-Pegs Glenoids
Applicant	Lima Corporate S.P.A.
Product code	KWS
Device class	Class II
Decision date	Apr 6, 2016
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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SMR 3-Pegs Glenoids

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