510(k) K070192 ยท FTL Mesh, Surgical, Polymeric
ATRIUM PROLITE ULTRA S MESH
| Applicant | Atrium Medical Corp., Hudson NH, US |
| Decision | Substantially Equivalent, Mar 8, 2007 |
| Received | Jan 22, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K070192
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.