Scholten Surgical Instruments, Inc.

Scholten Surgical Instruments, Inc. — FDA 510(k) Submissions

Scholten Surgical Instruments, Inc. has submitted 8 FDA 510(k) premarket notifications since 1985, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Permanent Pacemaker Electrode, Forceps, General & Plastic Surgery, Stand, Infusion, Retractor, System, X-ray, Angiographic . Use the specialty filter in the sidebar to narrow results.