K-number	K161120
Device name	SMR TT Metal Back Glenoid, Bone Graft instruments
Applicant	Lima Corporate S.P.A.
Product code	PHX
Device class	Class II
Decision date	Feb 21, 2017
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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SMR TT Metal Back Glenoid, Bone Graft instruments

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