Neuravi, Ltd. · Class II · Cleared Jul 30, 2021
| K-number | K211338 |
| Device name | EMBOTRAP III Revascularization Device |
| Applicant | Neuravi, Ltd. |
| Product code | NRY |
| Device class | Class II |
| Decision date | Jul 30, 2021 |
| 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