Nexstep Medical is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Nexstep Medical - FDA 510(k) Cleared Devices
Recent clearances: All’InCath 035M PTA Balloon Dilatation Catheter
1
Total
1
Cleared
0
Denied
Nexstep Medical has 1 FDA 510(k) cleared medical devices. Based in Dijon, FR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nexstep Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - Nexstep Medical
1 devices