510(k) K052070 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT IN ZIRCONIA, ATLANTIS GEMEINI + ABUTMENT IN ZIRCONIA
| Applicant | Atlantis Components, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Oct 14, 2005 |
| Received | Aug 1, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052070
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.