Neoligaments, Ltd.

Neoligaments, Ltd. — FDA 510(k) Submissions

Neoligaments, Ltd. has submitted 7 FDA 510(k) premarket notifications since 1990, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Staple, Fixation, Bone, Instrument, Surgical, Orthopedic, Ac-powered Motor And Accessory/attachment, Bit, Drill . Use the specialty filter in the sidebar to narrow results.