S.M.A.I.O

S.M.A.I.O — FDA 510(k) Submissions

S.M.A.I.O has submitted 9 FDA 510(k) premarket notifications since 2020, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Thoracolumbosacral Pedicle Screw System, System, Image Processing, Radiological . Use the specialty filter in the sidebar to narrow results.