Linvatec Corp.
Linvatec Corp. — FDA 510(k) Submissions
Linvatec Corp. has submitted 93 FDA 510(k) premarket notifications since 1992, of which 87 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Arthroscope, Screw, Fixation, Bone, Fastener, Fixation, Biodegradable, Soft Tissue, Fastener, Fixation, Nondegradable, Soft Tissue, Electrosurgical, Cutting & Coagulation & Accessories . Use the specialty filter in the sidebar to narrow results.
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