Zimmer Biomet

Zimmer Biomet — FDA 510(k) Submissions

Zimmer Biomet has submitted 5 FDA 510(k) premarket notifications since 2024, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer, Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented, Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented, Plate, Fixation, Bone, Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer . Use the specialty filter in the sidebar to narrow results.