Visionare, LLC · Class II · Cleared Dec 28, 2018
| K-number | K180204 |
| Device name | CranioMaxillofacial Fixation (CMF) System - CMF Visionare |
| Applicant | Visionare, LLC |
| Product code | JEY |
| Device class | Class II |
| Decision date | Dec 28, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 872.4760 |
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