Medical Device Manufacturer · US , Raynham , MA

DePuy Synthes - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1979

Recent clearances: DePuy Synthes Retrograde Femoral Nail Advanced System, CROSSNAV Navigation Enabled Instruments, Robotic Integration Instruments

19
Total
19
Cleared
0
Denied

DePuy Synthes has 19 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.

Latest FDA clearance: Aug 2024. Active since 1979.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Synthes GmbH as regulatory consultant.

FDA 510(k) Regulatory Record - DePuy Synthes

19 devices
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