510(k) K230794 ยท JXI Cuff, Nerve
Rebuilder Nerve Guidance Conduit
| Applicant | Celestray Biotech Company, LLC.,, Bethesda MD, US |
| Decision | Substantially Equivalent, Jan 29, 2024 |
| Received | Mar 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230794
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.