510(k) K200431 ยท FMF Syringe, Piston
3D GraftRasp System
| Applicant | Surgentec, Boca Raton FL, US |
| Decision | Substantially Equivalent, May 18, 2020 |
| Received | Feb 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200431
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.