Osteotomy Wedge System
Oct 2025
88d
Sinaptic Surgical
1
Total
1
Cleared
0
Denied
Sinaptic Surgical — FDA 510(k) Submissions
Sinaptic Surgical 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 Bone Wedge . Use the specialty filter in the sidebar to narrow results.
1 devices