510(k) K984220 ยท FTL Mesh, Surgical, Polymeric
MODIFICATION OF PROLENE (POLYPROPYLENE) HERNIA SYSTEM, NONABSORBABLE SYNTHETIC SURGICAL MESH
| Applicant | ETHICON, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Feb 23, 1999 |
| Received | Nov 25, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984220
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.