510(k) K170372 ยท DZE Implant, Endosseous, Root-Form
SpiralTech Dental Implant System
| Applicant | Spiraltech Superior Dental Implants, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jun 30, 2017 |
| Received | Feb 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170372
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.