Techfit Digital Surgery, Inc.

Techfit Digital Surgery, Inc. — FDA 510(k) Submissions

Techfit Digital Surgery, Inc. has submitted 4 FDA 510(k) premarket notifications since 2022, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Cranioplasty, Preformed, Alterable, Plate, Fixation, Bone, System, Image Processing, Radiological, Driver, Wire, And Bone Drill, Manual . Use the specialty filter in the sidebar to narrow results.