510(k) K922308 ยท FTM Mesh, Surgical
TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER
| Applicant | Ti-Mesh, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Jan 12, 1993 |
| Received | May 15, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922308
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.