510(k) K130221 ยท DZE Implant, Endosseous, Root-Form
HERO II DENTAL IMPLANT SYSTEM, UI DENTAL IMPLANT SYSTEM
| Applicant | Medimecca Co., Ltd., Anaheim CA, US |
| Decision | Substantially Equivalent, Mar 21, 2013 |
| Received | Jan 29, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130221
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.