510(k) K211132 ยท FTL Mesh, Surgical, Polymeric
ARISTE AB Mesh
| Applicant | Ariste Medical, LLC, Sandy UT, US |
| Decision | Substantially Equivalent, Mar 18, 2022 |
| Received | Apr 16, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211132
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.