510(k) K071439 ยท DZE Implant, Endosseous, Root-Form
ZIMMER PATIENT-SPECIFIC ABUTMENT, INTERNAL HEX, TITANIUM
| Applicant | Zimmer Dental, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Sep 20, 2007 |
| Received | May 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071439
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.