510(k) K040070 ยท KYI Prosthesis, Wrist, Carpal Trapezium
ARTELON SPACER CMC-1
| Applicant | Artimplant AB, Washington DC, US |
| Decision | Substantially Equivalent, Sep 21, 2004 |
| Received | Jan 14, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040070
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.