510(k) K002619 ยท JEY Plate, Bone
NEWGEN SYSTEM
| Applicant | Stryker Instruments, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Nov 16, 2000 |
| Received | Aug 23, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002619
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.