510(k) K113042 ยท DZE Implant, Endosseous, Root-Form
REVOIS IMPLANT SYSTEM
| Applicant | Riemser Arzneimittel AG, Durham NC, US |
| Decision | Substantially Equivalent, Mar 8, 2013 |
| Received | Oct 12, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113042
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.