510(k) K904350 ยท FZE Prosthesis, Nose, Internal
CUI DORSAL COLUMELLA PROSTHESIS
| Applicant | Cui Corp., Santa Barbara CA, US |
| Decision | Substantially Equivalent, Nov 26, 1990 |
| Received | Sep 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904350
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.