De Novo
DEN240014: ARC-EX System
FDA De Novo · onward medical inc. · decided Dec 19, 2024
Key facts
| De Novo number | DEN240014 |
|---|---|
| Device name | ARC-EX System |
| Applicant | onward medical inc. |
| Product code | SDO |
| Date received | Mar 28, 2024 |
| Decision date | Dec 19, 2024 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Physical Medicine |
| FEI number | 3027062639 |
At a glance
- 1–9 Later 510(k)s citing this De Novo
- 1–9 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: