510(k) K091208 ยท DZE Implant, Endosseous, Root-Form
GS III SYSTEM
| Applicant | Osstem Implant Co., Ltd., Fariless Hills PA, US |
| Decision | Substantially Equivalent, Mar 3, 2010 |
| Received | Apr 24, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091208
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.