Newclip Technics

Newclip Technics — FDA 510(k) Submissions

Newclip Technics has submitted 31 FDA 510(k) premarket notifications since 2006, of which 31 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Fixation, Bone, Screw, Fixation, Bone, Orthopaedic Surgical Planning And Instrument Guides, Pin, Fixation, Smooth . Use the specialty filter in the sidebar to narrow results.