Orthocon, Inc.

Orthocon, Inc. — FDA 510(k) Submissions

Orthocon, Inc. has submitted 33 FDA 510(k) premarket notifications since 2006, of which 33 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Wax, Bone, Filler, Bone Void, Calcium Compound, Methyl Methacrylate For Cranioplasty, Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) . Use the specialty filter in the sidebar to narrow results.