Peters Surgical

Peters Surgical — FDA 510(k) Submissions

Peters Surgical has submitted 7 FDA 510(k) premarket notifications since 2005, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Absorbable, Synthetic, Polyglycolic Acid, Suture, Nonabsorbable, Synthetic, Polypropylene, Suture, Nonabsorbable, Synthetic, Polyethylene, Suture, Surgical, Nonabsorbable, Poly (vinylidene Fluoride), Ring, Annuloplasty . Use the specialty filter in the sidebar to narrow results.