510(k) K161697 ยท PGW Ear, Nose, And Throat Stereotaxic Instrument
Acclarent NavWire Sinus Navigation Guidewire
| Applicant | Acclarent, Inc., Irvin CA, US |
| Decision | Substantially Equivalent, Oct 24, 2016 |
| Received | Jun 20, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161697
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.