510(k) K123870 ยท DZE Implant, Endosseous, Root-Form
XPEED ANYRIDGE INTERNAL IMPLANT SYSTEM
| Applicant | Megagen Implant Co., Ltd., Brea CA, US |
| Decision | Substantially Equivalent, Mar 27, 2013 |
| Received | Dec 17, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123870
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.