510(k) K162752 ยท FTM Mesh, Surgical
ARTIA Reconstructive Tissue Matrix Perforated
| Applicant | Lifecell Corporation, Branchburg NJ, US |
| Decision | Substantially Equivalent, Feb 24, 2017 |
| Received | Sep 30, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162752
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.