510(k) K191545 ยท FTL Mesh, Surgical, Polymeric
Exogenesis Hernia Mesh
| Applicant | Exogenesis Corporation, Billerica MA, US |
| Decision | Substantially Equivalent, Sep 26, 2019 |
| Received | Jun 11, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191545
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.