Corin USA

Corin USA — FDA 510(k) Submissions

Corin USA has submitted 57 FDA 510(k) premarket notifications since 1996, of which 57 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented, Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, System, Image Processing, Radiological, Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented, Orthosis, Spondylolisthesis Spinal Fixation . Use the specialty filter in the sidebar to narrow results.