510(k) K101004 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS ABUTMENT FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS GEMINI ABUTMENT, ATLANTIS GEMINI + ABUTMENT
| Applicant | Astra Tech, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Aug 16, 2010 |
| Received | Apr 12, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101004
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.