Pontis Orthopaedics, LLC

Pontis Orthopaedics, LLC — FDA 510(k) Submissions

Pontis Orthopaedics, LLC has submitted 2 FDA 510(k) premarket notifications since 2014, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Fastener, Fixation, Nondegradable, Soft Tissue, Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile . Use the specialty filter in the sidebar to narrow results.