Arthrocare System 15000 Contoller, Model 72202149, Arthrocare Arthrowands, Model 72202139,72202141, 72202143, 72202144

K090393 is the FDA 510(k) clearance record for ARTHROCARE SYSTEM 15000 CONTOLLER, MODEL 72202149, ARTHROCARE ARTHROWANDS, MODEL 72202139,72202141, 72202143, 72202144, a class II device, cleared for Arthrocare Corp. on 2009-06-23 under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 149 510(k) clearances for Arthrocare Corp., from 1995-03-13 to 2026-03-30. As of 2026-09-10, FDA records show no recalls naming K090393.