Medical Device Manufacturer · FR , Merignac

Satalec-Acteon Group - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017
1
Total
1
Cleared
0
Denied

Satalec-Acteon Group has 1 FDA 510(k) cleared medical devices. Based in Merignac, FR.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Satalec-Acteon Group Filter by specialty or product code using the sidebar.

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