510(k) K051652 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS ABUTMENT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI+ ABUTMENT
| Applicant | Atlantis Components, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Jul 22, 2005 |
| Received | Jun 21, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051652
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.