Wrightmedicaltechnologyinc

Wrightmedicaltechnologyinc — FDA 510(k) Submissions

Wrightmedicaltechnologyinc has submitted 302 FDA 510(k) premarket notifications since 1993, of which 291 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Fixation, Bone, Screw, Fixation, Bone, Filler, Bone Void, Calcium Compound, Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component), Prosthesis, Ankle, Semi-constrained, Cemented, Metal/polymer . Use the specialty filter in the sidebar to narrow results.