De Novo
DEN110019: NEBA SYSTEM
FDA De Novo · lexicor medical technology, llc · decided Jul 15, 2013
Key facts
| De Novo number | DEN110019 |
|---|---|
| Device name | NEBA SYSTEM |
| Applicant | lexicor medical technology, llc |
| Product code | NCG |
| Date received | Dec 8, 2011 |
| Decision date | Jul 15, 2013 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Neurology |
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: