TECHFIT DISRP? System
Jun 2023
142d
Techfit Digital Surgery
1
Total
1
Cleared
0
Denied
Techfit Digital Surgery — FDA 510(k) Submissions
Techfit Digital Surgery 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 Driver, Wire, And Bone Drill, Manual . Use the specialty filter in the sidebar to narrow results.
1 devices