Double Medical Technology, Inc.

Double Medical Technology, Inc. — FDA 510(k) Submissions

Double Medical Technology, Inc. has submitted 12 FDA 510(k) premarket notifications since 2016, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Screw, Fixation, Bone, Plate, Fixation, Bone, Rod, Fixation, Intramedullary And Accessories, Appliance, Fixation, Spinal Intervertebral Body, Posterior Cervical Screw System . Use the specialty filter in the sidebar to narrow results.