A.M. Surgical, Inc.

A.M. Surgical, Inc. — FDA 510(k) Submissions

A.M. Surgical, Inc. has submitted 6 FDA 510(k) premarket notifications since 1998, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Knife, Surgical, Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Metal Composite, Pin, Fixation, Smooth, Arthroscope, Screw, Fixation, Bone . Use the specialty filter in the sidebar to narrow results.