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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