510(k) K030839 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA)
| Applicant | Medtronic Ave, Inc., Santa Rosa CA, US |
| Decision | Unknown, May 30, 2003 |
| Received | Mar 17, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030839
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.