510(k) K171687 ยท LRC Instrument, Ent Manual Surgical
Relieva SpinPlus Nav Balloon Sinuplasty System
| Applicant | Acclarent, Inc., Irvin CA, US |
| Decision | Substantially Equivalent, Sep 5, 2017 |
| Received | Jun 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171687
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.