510(k) K230227 ยท FTL Mesh, Surgical, Polymeric
T-Line Hernia Mesh
| Applicant | Deep Blue Medical Advances, Inc., Durham NC, US |
| Decision | Substantially Equivalent, Feb 23, 2023 |
| Received | Jan 27, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230227
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.