510(k) K030378 ยท GXN Plate, Cranioplasty, Preformed, Non-Alterable
STRYKER LEIBINGER CRANIAL FIXATION SYSTEM
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Mar 20, 2003 |
| Received | Feb 5, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030378
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.