Medical Device Manufacturer · FR , Ecully

Spineway SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016
2
Total
2
Cleared
0
Denied

Spineway SA has 2 FDA 510(k) cleared medical devices. Based in Ecully, FR.

Historical record: 2 cleared submissions from 2016 to 2019. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Spineway SA

2 devices
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