Turbo-Elite Laser Atherectomy Catheter
Mar 2025
30d
Spectranetics
1
Total
1
Cleared
0
Denied
Spectranetics — FDA 510(k) Submissions
Spectranetics has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Peripheral, Atherectomy . Use the specialty filter in the sidebar to narrow results.
1 devices