510(k) K182293 ยท DZE Implant, Endosseous, Root-Form
OsseOne Dental Implant System
| Applicant | Synoross Dba Osseone, Glendale CA, US |
| Decision | Substantially Equivalent, Feb 15, 2019 |
| Received | Aug 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182293
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.