510(k) K171237 ยท HRX Arthroscope
FMS VUE II Fluid Management and Tissue Debridement System
| Applicant | Medos International SARL, Le Locle, CH |
| Decision | Substantially Equivalent, Jan 18, 2018 |
| Received | Apr 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171237
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.