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 |