Nexa Orthopedics, Inc.

Nexa Orthopedics, Inc. — FDA 510(k) Submissions

Nexa Orthopedics, Inc. has submitted 16 FDA 510(k) premarket notifications since 1997, of which 16 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Toe, Constrained, Polymer, Screw, Fixation, Bone, Pin, Fixation, Threaded, Plate, Fixation, Bone, Prosthesis, Wrist, Carpal Trapezium . Use the specialty filter in the sidebar to narrow results.