510(k) K110110 ยท FTL Mesh, Surgical, Polymeric
ATRIUM CENTRILFX MESH
| Applicant | Atrium Medical Corporation, Hudson NH, US |
| Decision | Substantially Equivalent, Feb 15, 2011 |
| Received | Jan 14, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110110
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.