510(k) K081302 ยท DZE Implant, Endosseous, Root-Form
RESCUE EXTERNAL IMPLANT SYSTEM
| Applicant | Megagen Implant Co., Ltd., Santa Fe Springs CA, US |
| Decision | Substantially Equivalent, Aug 15, 2008 |
| Received | May 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081302
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.