| K-number | K202780 |
| Device name | Sectum |
| Applicant | Neauvia North America |
| Product code | PBX |
| Device class | Class II |
| Decision date | Jul 30, 2021 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
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