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StealthStation Cranial Software v1.3.2

K203639 Class II Special
Decision Date
2021-01-13
Sponsor / Applicant
Medtronic Navigation, Inc.

Technical Specification

510(k) Submission ID K203639
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2021-01-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

StealthStation Cranial Software v1.3.2 received FDA 510(k) clearance under submission number K203639, sponsored by Medtronic Navigation, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2021-01-13.

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.