510(k) K222457 ยท DZE Implant, Endosseous, Root-Form
Provata Implant System
| Applicant | Southern Implants (Pty), Ltd., Guateng, ZA |
| Decision | Substantially Equivalent, Mar 6, 2023 |
| Received | Aug 15, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222457
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.