meddevicedb.com FDA Device Reference

Stealth-Midas System

K160713 Class II Traditional
Decision Date
2016-05-26
Sponsor / Applicant
Medtronic Powered Surgical Solutions

Technical Specification

510(k) Submission ID K160713
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2016-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Stealth-Midas System received FDA 510(k) clearance under submission number K160713, sponsored by Medtronic Powered Surgical Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2016-05-26.

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.