510(k) K192218 ยท NHA Abutment, Implant, Dental, Endosseous
Custom Legacy and Custom InterActive Titanium Abutments
| Applicant | Implant Direct Sybron Manufacturing, LLC, Thousand Oaks CA, US |
| Decision | Substantially Equivalent, May 8, 2020 |
| Received | Aug 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192218
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.