Pmt Corp.

Pmt Corp. — FDA 510(k) Submissions

Pmt Corp. has submitted 20 FDA 510(k) premarket notifications since 1988, of which 20 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Shunt, Central Nervous System And Components, Elastomer, Silicone, For Scar Management, Electrode, Depth, Electrode, Cortical, Spatula, Surgical, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.