510(k) K061954 ยท KYI Prosthesis, Wrist, Carpal Trapezium
ARTELON CMC SPACER ARTHRO
| Applicant | Artimplant AB, Washington DC, US |
| Decision | Substantially Equivalent, Jun 1, 2007 |
| Received | Jul 11, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061954
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.