Fortimedix Surgical B.V. is one of 144 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Fortimedix Surgical B.V. - FDA 510(k) Cleared Devices
Recent clearances: FMX314 Surgical Platform
1
Total
1
Cleared
0
Denied
Fortimedix Surgical B.V. has 1 FDA 510(k) cleared medical devices. Based in Nuth, NL.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Fortimedix Surgical B.V. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Fortimedix Surgical B.V.
1 devices