Dow Corning Wright

Dow Corning Wright — FDA 510(k) Submissions

Dow Corning Wright has submitted 74 FDA 510(k) premarket notifications since 1979, of which 52 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented, Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented, Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer, Prosthesis, Hip, Semi-constrained, Uncemented, Metal / Polymer, Non-porous, Calcium Phosphate . Use the specialty filter in the sidebar to narrow results.