K190672 is an FDA 510(k) clearance for the StealthStation Synergy Cranial S7 Software v.2.2.8, StealthStation Cranial Software v3.1.1. This device is classified as a Neurological Stereotaxic Instrument (Class II - Special Controls, product code HAW).
Submitted by Medtronic Navigation, Inc. (Louisville, US). The FDA issued a Cleared decision on July 31, 2019, 138 days after receiving the submission on March 15, 2019.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.4560.
| 510(k) Number | K190672 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 15, 2019 |
| Decision Date | July 31, 2019 |
| Days to Decision | 138 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | HAW — Neurological Stereotaxic Instrument |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.4560 |