510(k) K082523 ยท EKX Handpiece, Direct Drive, Ac-Powered
OSSTELL ISQ IMPLANT STABILITY METER
| Applicant | Osstell AB, Alexandria VA, US |
| Decision | Substantially Equivalent, Sep 26, 2008 |
| Received | Sep 2, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082523
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.