510(k) K061956 ยท KYI Prosthesis, Wrist, Carpal Trapezium
ARTELON STT SPACER
| Applicant | Artimplant AB, Washington DC, US |
| Decision | Substantially Equivalent, Jun 7, 2007 |
| Received | Jul 11, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061956
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.