510(k) K191238 ยท HSB Rod, Fixation, Intramedullary And Accessories
Zimmer Guide Wire Devices
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 5, 2019 |
| Received | May 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191238
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.