Medcanica, Inc.

Medcanica, Inc. — FDA 510(k) Submissions

Medcanica, Inc. has submitted 5 FDA 510(k) premarket notifications since 1999, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Trocar, Pin, Fixation, Smooth, Device, Biopsy, Endomyocardial . Use the specialty filter in the sidebar to narrow results.