510(k) K242432 ยท DZI Drill, Bone, Powered
MT-Bone
| Applicant | Mectron S.P.A., Carasco, IT |
| Decision | Substantially Equivalent, Aug 19, 2024 |
| Received | Aug 16, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242432
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.