510(k) K183472 · FTM Mesh, Surgical
DePuy Synthes Porous Polyethylene Implants and Titanium Wires Portfolio MR Conditional
| Applicant | Synthes (USA) Products, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Mar 13, 2019 |
| Received | Dec 14, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183472
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.