De Novo
DEN120017: Medtronic DUET External Drainage and Monitoring System
FDA De Novo · medtronic neurosurgery · decided Aug 22, 2014
Key facts
| De Novo number | DEN120017 |
|---|---|
| Device name | Medtronic DUET External Drainage and Monitoring System |
| Applicant | medtronic neurosurgery |
| Product code | PCB |
| Date received | Dec 21, 2012 |
| Decision date | Aug 22, 2014 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Neurology |
| FEI number | 2021898 |
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: