510(k) K172395 · FTL Mesh, Surgical, Polymeric
Duatene bilayer mesh
| Applicant | Sofradim Production, Trévoux, FR |
| Decision | Substantially Equivalent, Feb 1, 2018 |
| Received | Aug 8, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172395
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.