Medcad

Medcad — FDA 510(k) Submissions

Medcad has submitted 8 FDA 510(k) premarket notifications since 2020, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Orthopaedic Surgical Planning And Instrument Guides, Driver, Wire, And Bone Drill, Manual, Plate, Bone, Plate, Cranioplasty, Preformed, Non-alterable . Use the specialty filter in the sidebar to narrow results.