The following data is part of a premarket notification filed by Medtronic Navigation, Inc. with the FDA for Stealthstation S8 System Platforms And Stealthstation Cranial Software.
Device ID | K162309 |
510k Number | K162309 |
Device Name: | StealthStation S8 System Platforms And StealthStation Cranial Software |
Classification | Neurological Stereotaxic Instrument |
Applicant | MEDTRONIC NAVIGATION, INC. 826 COAL CREEK CIRCLE Louisville, CO 80027 |
Contact | Tia Fushimi-bain |
Correspondent | Tia Fushimi-bain MEDTRONIC NAVIGATION, INC. 826 COAL CREEK CIRCLE Louisville, CO 80027 |
Product Code | HAW |
Subsequent Product Code | OLO |
Subsequent Product Code | PGW |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-08-17 |
Decision Date | 2017-03-31 |
Summary: | summary |