510(k) K251970 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
Sprinter Legend Rapid Exchange Balloon Dilatation Catheter
| Applicant | Medtronic, Ireland, Galway, IE |
| Decision | Substantially Equivalent, Jan 17, 2026 |
| Received | Jun 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251970
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.