Zimmer Switzerland Manufacturing GmbH

Zimmer Switzerland Manufacturing GmbH — FDA 510(k) Submissions

Zimmer Switzerland Manufacturing GmbH has submitted 4 FDA 510(k) premarket notifications since 2021, of which 4 received clearance as substantially equivalent to a predicate device.

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