510(k) K250075 ยท DQX Wire, Guide, Catheter
Medtronic Stedi Extra Support Guidewire
| Applicant | Medtronic, Inc., Miinneapolis MN, US |
| Decision | Substantially Equivalent, Jun 13, 2025 |
| Received | Jan 10, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250075
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.