510(k) K072483 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS ABUTMENT IN ZIRCONIA FOR 3I CERTAIN MICROAMINI IMPLANTS, GEMINI ABUTMENT IN ZIRCONIA FOR ASTRA IMPLANTS
| Applicant | Atlantis Components, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Nov 16, 2007 |
| Received | Sep 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072483
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.