510(k) K233368 ยท FMF Syringe, Piston
Allograft Delivery Device (OFAC-C)
| Applicant | Bioventus, LLC, Durham NC, US |
| Decision | Substantially Equivalent, Jun 25, 2024 |
| Received | Oct 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233368
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.