Fixier S.A. DE C.V. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Fixier S.A. DE C.V. has 1 FDA 510(k) cleared medical devices. Based in Leon, MX.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Fixier S.A. DE C.V. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aurelia Brownridge as regulatory consultant.
FDA 510(k) Regulatory Record - Fixier S.A. DE C.V.
1 devices