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FDA 510(k) Applications Submitted by Limacorporate
FDA 510(k) Number
Submission Date
Device Name
Applicant
K243809
12/11/2024
Biolox« Delta Revision heads
Limacorporate
K190911
04/08/2019
Physica KR Liner and SMR Reverse Humeral Liner
LimaCorporate
K211938
06/23/2021
Physica LMC Knee System
LimaCorporate
K213785
12/06/2021
SMR TT Hybrid Glenoid, SMR 3-Pegs Cemented Glenoid
LimaCorporate
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