Anika Therapeutics, Inc.

Anika Therapeutics, Inc. — FDA 510(k) Submissions

Anika Therapeutics, Inc. has submitted 9 FDA 510(k) premarket notifications since 2017, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filler, Bone Void, Calcium Compound, Mesh, Surgical, Non-absorbable, Orthopaedics, Reinforcement Of Tendon, Staple, Implantable, Fastener, Fixation, Nondegradable, Soft Tissue . Use the specialty filter in the sidebar to narrow results.