Spinemed Ges.M.B.H is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Spinemed Ges.M.B.H - FDA 510(k) Cleared Devices
Recent clearances: ACRON™ TLIF System
1
Total
1
Cleared
0
Denied
Spinemed Ges.M.B.H has 1 FDA 510(k) cleared medical devices. Based in Wien, AT.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinemed Ges.M.B.H Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Spinemed Ges.M.B.H
1 devices