510(k) K240535 ยท HRX Arthroscope
Digital ClarusScope System; Digital NeuroPEN System
| Applicant | Clarus Medical, LLC, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 25, 2024 |
| Received | Feb 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240535
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.