Riverpoint Medical

Riverpoint Medical — FDA 510(k) Submissions

Riverpoint Medical has submitted 27 FDA 510(k) premarket notifications since 2009, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Fastener, Fixation, Nondegradable, Soft Tissue, Suture, Nonabsorbable, Synthetic, Polyethylene, Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene, Plug, Punctum, Suture, Nonabsorbable, Synthetic, Polyamide . Use the specialty filter in the sidebar to narrow results.