Medical Device Manufacturer · CH , Castel San Pietro (Ch)

Medacta Inernational SA - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2020
4
Total
4
Cleared
0
Denied

Medacta Inernational SA has 4 FDA 510(k) cleared medical devices. Based in Castel San Pietro (Ch), CH.

Last cleared in 2021. Active since 2020. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Medacta Inernational SA Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Medacta USA as regulatory consultant.

FDA 510(k) Regulatory Record - Medacta Inernational SA

4 devices
1-4 of 4
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All4 Orthopedic 4