Spineworxx AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Spineworxx AG - FDA 510(k) Cleared Devices
Recent clearances: Born PT-LIF Cage HA
1
Total
1
Cleared
0
Denied
Spineworxx AG has 1 FDA 510(k) cleared medical devices. Based in St. Gallen, CH.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spineworxx AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spineworxx AG
1 devices