EVac 70 Xtra Plasma Wand with Integrated Cable, PROcise XP Plasma Wand with Integrated Cable

K142999 is the FDA 510(k) clearance record for EVac 70 Xtra Plasma Wand with Integrated Cable, PROcise XP Plasma Wand with Integrated Cable, a class II device, cleared for ArthroCare Corporation on 2014-11-19 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 Corporation, from 1995-03-13 to 2026-03-30. As of 2026-09-10, FDA records show 3 recalls naming K142999.