FDA 510(k) Applications Submitted by Marc Chaunet

FDA 510(k) Number Submission Date Device Name Applicant
K181302 05/17/2018 Bodycad Unicompartmental Knee System Bodycad Laboratories Inc.
K191907 07/16/2019 OptoWire III Opsens Inc.
K192340 08/28/2019 OptoMonitor Opsens Inc
K202943 09/30/2020 OptoMonitor 3 Opsens Inc.
K213854 12/10/2021 SavvyWire Opsens Inc.
K193620 12/26/2019 OptoMonitor 3 Opsens Inc.
K163700 12/29/2016 Bodycad Unicompartmental Knee System Bodycad Laboratories, Inc.


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