510(k) K172636 ยท FTL Mesh, Surgical, Polymeric
VitaMESH Macroporous PP Surgical Mesh
| Applicant | Proxy Biomedical , Ltd., Galway, IE |
| Decision | Substantially Equivalent, Apr 30, 2018 |
| Received | Sep 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172636
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.