| K-number | K172167 |
| Device name | Zenith Flex System |
| Applicant | Inneuroco, Inc. |
| Product code | NRY |
| Device class | Class II |
| Decision date | Apr 19, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 870.1250 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov