Pytheas Navigation Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Pytheas Navigation Sas - FDA 510(k) Cleared Devices
Recent clearances: Pytheas Your Guided Trajectory
1
Total
1
Cleared
0
Denied
Pytheas Navigation Sas has 1 FDA 510(k) cleared medical devices. Based in Marseille, FR.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pytheas Navigation Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pytheas Navigation Sas
1 devices