510(k) K122295 ยท NHA Abutment, Implant, Dental, Endosseous
CORE 3D ABUTMENT SYSTEM FOR DIGITAL PROSTHETIC SOLUTIONS
| Applicant | Core 3D Protech, S.L., Santpedor, ES |
| Decision | Substantially Equivalent, Oct 24, 2013 |
| Received | Jul 31, 2012 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K122295
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.