510(k) K171817 ยท FTM Mesh, Surgical
Biodesign Diaphragmatic Hernia Graft
| Applicant | Cook Biotech Incorporated, West Lafayette IN, US |
| Decision | Substantially Equivalent, Mar 13, 2018 |
| Received | Jun 19, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171817
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.