510(k) K170675 ยท FMF Syringe, Piston
Graftgun Universal Graft Delivery System
| Applicant | SurGenTec, LLC, Boca Raton FL, US |
| Decision | Substantially Equivalent, Jul 19, 2017 |
| Received | Mar 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170675
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.