Zimmer Medizinsysteme GmbH

Zimmer Medizinsysteme GmbH — FDA 510(k) Submissions

Zimmer Medizinsysteme GmbH has submitted 13 FDA 510(k) premarket notifications since 2016, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Muscle, Powered, For Muscle Conditioning, Massager, Vacuum, Radio Frequency Induced Heat, Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat, Stimulator, Muscle, Powered, Powered Laser Surgical Instrument . Use the specialty filter in the sidebar to narrow results.