510(k) K072959 ยท DZE Implant, Endosseous, Root-Form
MS SYSTEM (DENTURE)
| Applicant | Osstem Implant Co., Ltd., Fairless Hills PA, US |
| Decision | Substantially Equivalent, Feb 4, 2008 |
| Received | Oct 19, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072959
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.