510(k) K103020 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT
| Applicant | Atlantis Components, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Feb 3, 2011 |
| Received | Oct 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103020
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.