510(k) K002093 ยท FTL Mesh, Surgical, Polymeric
ATRIUM LITE MESH
| Applicant | Atrium Medical Corp., Hudson NH, US |
| Decision | Substantially Equivalent, Jul 24, 2000 |
| Received | Jul 11, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K002093
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.