Finesse Injectable? PTA Balloon Dilatation Catheter
Jul 2024
29d
Summa Therapeutics
1
Total
1
Cleared
0
Denied
Summa Therapeutics — FDA 510(k) Submissions
Summa Therapeutics has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Angioplasty, Peripheral, Transluminal . Use the specialty filter in the sidebar to narrow results.
1 devices