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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