510(k) K150712 ยท FTM Mesh, Surgical
LTM-Perforated Surgical Mesh
| Applicant | Lifecell Corporation, Branchburg NJ, US |
| Decision | Substantially Equivalent, Jul 2, 2015 |
| Received | Mar 19, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150712
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.