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# Medtronic Accurian RF Ablation Platform Cleared
- URL: https://www.fdaweb.com/medtronic-accurian-rf-ablation-platform-cleared/
- Published: 2019-02-27T12:00:00.000Z
- Updated: 2026-09-15T01:08:15.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5143488

FDA has cleared a Medtronic 510(k) for the Accurian RF ablation platform for use in radio frequency ablation of nerve tissues for treating pain. The device “combines proprietary hardware and quad core processing with advanced software for power and temperature control resulting in consistent and predictable lesion formation,” the company says. It can perform standard, pulsed, and enhanced procedures using internally-cooled probes to create a comprehensive range of lesion shapes, sizes, and volumes, it says.