510(k) K063058 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
ARTHREX ANATOEMIC PHALANGEAL PROSTHESIS
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Jan 3, 2007 |
| Received | Oct 5, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063058
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.