510(k) K241990 ยท HRX Arthroscope
SpineSite Endoscope System
| Applicant | Hydrocision, Inc., North Billerica MA, US |
| Decision | Substantially Equivalent, Jul 30, 2025 |
| Received | Jul 8, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241990
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.