510(k) K002699 ยท FTL Mesh, Surgical, Polymeric
PARIETEX COMPOSITE (PCO) MESH
| Applicant | Medical Device Consultants, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Feb 15, 2001 |
| Received | Aug 30, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002699
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.