Zinnanti Surgical Instruments, Inc.

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

Zinnanti Surgical Instruments, Inc. has submitted 76 FDA 510(k) premarket notifications since 1984, of which 76 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Manual, Specialized Obstetric-gynecologic, Laparoscope, General & Plastic Surgery, Scissors, General, Surgical, Cannula, Manipulator/injector, Uterine, Instrument, Manual, General Obstetric-gynecologic . Use the specialty filter in the sidebar to narrow results.