510(k) K993990 ยท GXN Plate, Cranioplasty, Preformed, Non-Alterable
LEIBINGER QUIK DISK TITANIUM CLAMP SYSTEM
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Feb 22, 2000 |
| Received | Nov 24, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993990
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.