510(k) K090260 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS
| Applicant | Straumann Manufacturing, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Feb 26, 2009 |
| Received | Feb 3, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090260
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.