Arthrocare Corp.
Arthrocare Corp. — FDA 510(k) Submissions
Arthrocare Corp. has submitted 112 FDA 510(k) premarket notifications since 1995, of which 112 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Fastener, Fixation, Nondegradable, Soft Tissue, Arthroscope, Cement, Bone, Vertebroplasty, Electrode, Electrosurgical, Active, Urological . Use the specialty filter in the sidebar to narrow results.
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