K-number	K233712
Device name	PRIMA Humeral System; PRIMA TT Glenoid
Applicant	Lima Corporate S.P.A.
Product code	MBF
Device class	Class II
Decision date	Jan 11, 2024
Decision	Substantially Equivalent
Regulation	888.3670

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View the full FDA submission: accessdata.fda.gov

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PRIMA Humeral System; PRIMA TT Glenoid

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