510(k) K233675 · HRX Arthroscope
FMS VUE Fluid Management and Tissue Debridement System
| Applicant | DePuy Mitek, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Feb 26, 2024 |
| Received | Nov 16, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233675
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.