Composite Removable Sinus Stent System
Dec 2017
262d
Sts Medical
1
Total
1
Cleared
0
Denied
Sts Medical — FDA 510(k) Submissions
Sts Medical has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Splint, Intranasal Septal . Use the specialty filter in the sidebar to narrow results.
1 devices