510(k) K143011 ยท DZE Implant, Endosseous, Root-Form
2014 InterActive/SwishActive System
| Applicant | Implant Direct Sybron Manufacturing, LLC, Thousand Oaks CA, US |
| Decision | Substantially Equivalent, Jul 16, 2015 |
| Received | Oct 20, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143011
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.