510(k) K221673 ยท NHA Abutment, Implant, Dental, Endosseous
Bonafix TiBase
| Applicant | Zentek Medical, LLC, Manalapan NJ, US |
| Decision | Substantially Equivalent, Jul 14, 2023 |
| Received | Jun 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221673
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.