Vesitec Medical, Inc.

Vesitec Medical, Inc. — FDA 510(k) Submissions

Vesitec Medical, Inc. has submitted 3 FDA 510(k) premarket notifications since 1993, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Staple, Fixation, Bone, Surgical Instruments, G-u, Manual (and Accessories) . Use the specialty filter in the sidebar to narrow results.