510(k) K132219 ยท NHA Abutment, Implant, Dental, Endosseous
STRAUMANN(R) VARIOBASE(TM) ABUTMENT NNC, STRAUMANN(R) VARIOBASE(TM) ABUTMENT RN, STRAUMANN(R) VARIOBASE(TM) ABUTMENT WN,
| Applicant | Straumann USA, LLC, Andover MA, US |
| Decision | Substantially Equivalent, Feb 21, 2014 |
| Received | Jul 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132219
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.