Overture Resurfacing, Inc.

Overture Resurfacing, Inc. — FDA 510(k) Submissions

Overture Resurfacing, Inc. has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer, Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer . Use the specialty filter in the sidebar to narrow results.