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FDA 510(k) Applications Submitted by Exactech Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K240393
02/08/2024
Exactech« TRULIANT« Knee System
Exactech Inc.
K232002
07/05/2023
Vantage« Total Ankle System
Exactech Inc.
K233482
10/26/2023
Equinoxe« Central Screw Baseplate System
Exactech Inc.
K180632
03/12/2018
Exactech Equinoxe Small Reverse Shoulder System
Exactech Inc.
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