Surgical Navigation Technologies, Inc.

Surgical Navigation Technologies, Inc. — FDA 510(k) Submissions

Surgical Navigation Technologies, Inc. has submitted 27 FDA 510(k) premarket notifications since 1996, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Neurological Stereotaxic Instrument, Accelerator, Linear, Medical, System, Image Processing, Radiological, System, Digital Image Communications, Radiological, Arthroscope . Use the specialty filter in the sidebar to narrow results.