510(k) K233800 ยท HRX Arthroscope
Vertos mild Device Kit (MDK-0002)
| Applicant | Vertos Medical, Inc., Aliso Viejo CA, US |
| Decision | Substantially Equivalent, May 6, 2024 |
| Received | Nov 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233800
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.