510(k) K173575 ยท DZE Implant, Endosseous, Root-Form
OsteoReady Dental Implant System
| Applicant | Osteoready, LLC, Concord MA, US |
| Decision | Substantially Equivalent, Aug 17, 2018 |
| Received | Nov 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173575
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.