510(k) K163212 · FTL Mesh, Surgical, Polymeric
Parietene DS Composite Mesh
| Applicant | Sofradim Production, Trévoux, FR |
| Decision | Substantially Equivalent, Jun 29, 2017 |
| Received | Nov 16, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163212
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.