Ultra? Compression Screw System
Nov 2025
169d
Pace Surgical
1
Total
1
Cleared
0
Denied
Pace Surgical — FDA 510(k) Submissions
Pace 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 Screw, Fixation, Bone . Use the specialty filter in the sidebar to narrow results.
1 devices