510(k) K142890 ยท NHA Abutment, Implant, Dental, Endosseous
Straumann Variobase Abutment NNC, Straumann Variobase Abutment RN, Straumann Variobase Abutment WN, Straumann Variobase Abutment NC, Straumann Variobase Abutment RC, IPS e.max CAD MO Coping, IPS e.max CAD LT Crown, IPS e.max CAD HT Crown, coron CoCr Single Unit
| Applicant | Straumann USA, LLC, Andover MA, US |
| Decision | Substantially Equivalent, Jan 9, 2015 |
| Received | Oct 3, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142890
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.