510(k) K200606 ยท FMF Syringe, Piston
O-Genesis Graft Delivery System
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, May 1, 2020 |
| Received | Mar 9, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200606
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.