Medical Device Manufacturer · FR , Strasbourg

Sc Medica

3 submissions · 3 cleared · Since 2024
3
Total
3
Cleared
0
Denied

Sc Medica — FDA 510(k) Submissions

Sc Medica has submitted 3 FDA 510(k) premarket notifications since 2024, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Facet Screw Spinal Device . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
All3 Orthopedic 3