510(k) K172240 ยท DZE Implant, Endosseous, Root-Form
SPI Dental Implant System
| Applicant | Msi France, Paris, FR |
| Decision | Substantially Equivalent, Jan 31, 2018 |
| Received | Jul 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172240
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.