Ignite Orthomotion

Ignite Orthomotion — FDA 510(k) Submissions

Ignite Orthomotion has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Femorotibial, Unicompartmental/unicondylar, Uncemented, Porous-coated, Metal/polymer . Use the specialty filter in the sidebar to narrow results.