Suturtek Incorporated

Suturtek Incorporated — FDA 510(k) Submissions

Suturtek Incorporated has submitted 4 FDA 510(k) premarket notifications since 2003, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile, Suture, Absorbable, Natural . Use the specialty filter in the sidebar to narrow results.