510(k) K241259 ยท MMX Device, Percutaneous Retrieval
Amplatz Goose Neck Snare Kit
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 3, 2024 |
| Received | May 6, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241259
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.