Cmf Medicon Surgical, Inc.

Cmf Medicon Surgical, Inc. — FDA 510(k) Submissions

Cmf Medicon Surgical, Inc. has submitted 4 FDA 510(k) premarket notifications since 2019, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spinal Vertebral Body Replacement Device, Spinal Vertebral Body Replacement Device - Cervical, Prosthesis, Nose, Internal, Thoracolumbosacral Pedicle Screw System . Use the specialty filter in the sidebar to narrow results.