510(k) K182957 ยท OTD Endovascular Suturing System
Heli-FX EndoAnchor System
| Applicant | Medtronic Vascular, Inc., Santa Rosa CA, US |
| Decision | Substantially Equivalent, Nov 21, 2018 |
| Received | Oct 24, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182957
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.