510(k) K972412 ยท FTL Mesh, Surgical, Polymeric
PROLENE POLYPROPYLENE MESH HERNIA DEVICE NONABSORBABLE SYNTHETIC SURGICAL MESH
| Applicant | ETHICON, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Sep 10, 1997 |
| Received | Jun 26, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972412
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.