Howmedica Corp.

Howmedica Corp. — FDA 510(k) Submissions

Howmedica Corp. has submitted 373 FDA 510(k) premarket notifications since 1976, of which 325 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented, Rod, Fixation, Intramedullary And Accessories, Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Plate, Fixation, Bone . Use the specialty filter in the sidebar to narrow results.