De Novo
DEN230025: MIRA Surgical System
FDA De Novo · virtual incision · decided Feb 23, 2024
Key facts
| De Novo number | DEN230025 |
|---|---|
| Device name | MIRA Surgical System |
| Applicant | virtual incision |
| Product code | SAB |
| Date received | Apr 11, 2023 |
| Decision date | Feb 23, 2024 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | General & Plastic Surgery |
| FEI number | 3030285773 |
At a glance
- 1–9 Later 510(k)s citing this De Novo
- 10–99 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
- No Decision summary on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About De Novo classification requests
The De Novo pathway classifies novel low- to moderate-risk devices that have no legally marketed predicate; each granted request creates a new classification regulation and product code.
Source: U.S. Food and Drug Administration (FDA), De Novo database · Source date: