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StealthStation S8 System Platforms and StealthStation Cranial Software

K162309 Class II Traditional
Decision Date
2017-03-31
Sponsor / Applicant
Medtronic Navigation, Inc.

Technical Specification

510(k) Submission ID K162309
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2017-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

StealthStation S8 System Platforms and StealthStation Cranial Software received FDA 510(k) clearance under submission number K162309, sponsored by Medtronic Navigation, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-03-31.

Classification & Regulation

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