510(k) K220142 ยท KYJ Prosthesis, Finger, Constrained, Polymer
BRM Digitalis Spacer
| Applicant | Brm Extremities Srl, Civate, IT |
| Decision | Substantially Equivalent, Apr 4, 2023 |
| Received | Jan 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220142
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.