Lp Arthroscopic Thigh Holding Device

K864513 is the FDA 510(k) clearance record for LP ARTHROSCOPIC THIGH HOLDING DEVICE, a class II device, cleared for Twin Falls Orthopedic Associates, P.A. on 1986-11-25 under FDA product code HRX (Arthroscope). FDA's definition for product code HRX 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 one 510(k) clearance for Twin Falls Orthopedic Associates, P.A. As of 2026-09-10, FDA records show no recalls naming K864513.