Zimmer Trabecular

Zimmer Trabecular — FDA 510(k) Submissions

Zimmer Trabecular has submitted 10 FDA 510(k) premarket notifications since 2004, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented, Spinal Vertebral Body Replacement Device, Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer, Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented . Use the specialty filter in the sidebar to narrow results.