Transdiscal System (Transdiscal Probe), Model Tdp-17-150-6

K031951 is the FDA 510(k) clearance record for TRANSDISCAL SYSTEM (TRANSDISCAL PROBE), MODEL TDP-17-150-6, a class II device, cleared for Baylis Medical Co., Inc. on 2003-09-11 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 53 510(k) clearances for Baylis Medical Co., Inc., from 1998-07-17 to 2025-05-29. As of 2026-09-10, FDA records show no recalls naming K031951.