K-number	K231099
Device name	SMR Hybrid Glenoid System
Applicant	Lima Corporate S.P.A.
Product code	MBF
Device class	Class II
Decision date	Dec 21, 2023
Decision	Substantially Equivalent
Regulation	888.3670

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Source

View the full FDA submission: accessdata.fda.gov

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SMR Hybrid Glenoid System

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