510(k) K062458 ยท KAM Cannula, Sinus
ETHMOID SINUS SPACER
| Applicant | Acclarent, Inc., Rmenlo Park CA, US |
| Decision | Substantially Equivalent, Sep 15, 2006 |
| Received | Aug 23, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062458
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.