510(k) K120338 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIA
| Applicant | Astra Tech, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Jul 5, 2012 |
| Received | Feb 3, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120338
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.