meddevicedb.com FDA Device Reference

Midas Rex Attachments and Dissecting Tools

K202552 Class II Traditional
Decision Date
2020-11-02
Sponsor / Applicant
Medtronic Powered Surgical Solutions (Mpss)

Technical Specification

510(k) Submission ID K202552
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2020-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Midas Rex Attachments and Dissecting Tools received FDA 510(k) clearance under submission number K202552, sponsored by Medtronic Powered Surgical Solutions (Mpss). The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2020-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.