510(k) K923419 ยท JEY Plate, Bone
TISMESH SYSTEM
| Applicant | Ti-Mesh, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Apr 8, 1993 |
| Received | Jul 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923419
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.