meddevicedb.com FDA Device Reference

SureTune4 Software

DEN210003 Class II Direct
Decision Date
2021-08-23
Sponsor / Applicant
Medtronic Neuromodulation

Technical Specification

510(k) Submission ID DEN210003
Product Code QQC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5855
Decision Date 2021-08-23
Clearance Pathway Direct

Official Documentation

No FDA summary/statement PDF is linked for this clearance in the current dataset. Consult the product code and regulation citation above to locate predicate documentation.

Clearance Summary

SureTune4 Software received FDA 510(k) clearance under submission number DEN210003, sponsored by Medtronic Neuromodulation. The device was reviewed via the Direct premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2021-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code QQC and 21 CFR 882.5855, within the Neurology review panel as a Class II device.