510(k) K241895 ยท SCY Sacroiliac Joint Guidewire Placement Device
Cannulated PsiFGuard
| Applicant | Spineguard, Vincennes, FR |
| Decision | Substantially Equivalent, Sep 26, 2024 |
| Received | Jun 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241895
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.