510(k) K260156 ยท HRX Arthroscope
TruVision Single-Use 1.9mm Arthroscopy System
| Applicant | Nexus CMF, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 9, 2026 |
| Received | Jan 20, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260156
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.