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 |