510(k) K143337 ยท NHA Abutment, Implant, Dental, Endosseous
CONELOG Titanium base CAD/CAM
| Applicant | Altatec GmbH, Wimsheim, DE |
| Decision | Substantially Equivalent, Feb 17, 2015 |
| Received | Nov 20, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143337
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.