Spinewelding AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Spinewelding AG - FDA 510(k) Cleared Devices
Recent clearances: Elaris Pedicle Screw System
1
Total
1
Cleared
0
Denied
Spinewelding AG has 1 FDA 510(k) cleared medical devices. Based in Schlieren, CH.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinewelding AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Spinewelding AG
1 devices