510(k) K230211 ยท PBJ Cranial Distraction System
CranioXpand
| Applicant | KLS-Martin L.P., Jacksonville FL, US |
| Decision | Substantially Equivalent, Nov 21, 2023 |
| Received | Jan 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230211
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.