510(k) K040022 ยท HRS Plate, Fixation, Bone
STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM
| Applicant | Stryker Leibinger, Kalamazoo MI, US |
| Decision | Substantially Equivalent, Mar 12, 2004 |
| Received | Jan 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040022
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.