510(k) K230623 ยท HRS Plate, Fixation, Bone
KITE Distal Fibula Kit
| Applicant | Intrauma S.P.A, Rivoli (To), IT |
| Decision | Substantially Equivalent, Sep 1, 2023 |
| Received | Mar 6, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230623
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.