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StealthStation Synergy Cranial S7 Software v.2.2.8, StealthStation Cranial Software v3.1.1

K190672 Class II Traditional
Decision Date
2019-07-31
Sponsor / Applicant
Medtronic Navigation, Inc.

Technical Specification

510(k) Submission ID K190672
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2019-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

StealthStation Synergy Cranial S7 Software v.2.2.8, StealthStation Cranial Software v3.1.1 received FDA 510(k) clearance under submission number K190672, 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 2019-07-31.

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.