510(k) K213631 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Chocolate PTA Balloon Catheter
| Applicant | Medtronic, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Dec 15, 2021 |
| Received | Nov 17, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213631
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.