Conmed Linvatec

Conmed Linvatec — FDA 510(k) Submissions

Conmed Linvatec has submitted 21 FDA 510(k) premarket notifications since 2005, of which 21 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Arthroscope, Screw, Fixation, Bone, Fastener, Fixation, Nondegradable, Soft Tissue, Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, Fastener, Fixation, Biodegradable, Soft Tissue . Use the specialty filter in the sidebar to narrow results.