Osteoremedies, LLC

Osteoremedies, LLC — FDA 510(k) Submissions

Osteoremedies, LLC has submitted 11 FDA 510(k) premarket notifications since 2015, of which 11 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Hip, Hemi-, Femoral, Metal, Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Bone Cement, Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented . Use the specialty filter in the sidebar to narrow results.