Huvex Interspinous Fusion System
Mar 2023
80d
Dio Medical Corp.
1
Total
1
Cleared
0
Denied
Dio Medical Corp. — FDA 510(k) Submissions
Dio Medical Corp. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Spinous Process Plate . Use the specialty filter in the sidebar to narrow results.
1 devices