510(k) K070052 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION
| Applicant | Vilex, Inc., Pleasant Hills PA, US |
| Decision | Substantially Equivalent, Mar 28, 2007 |
| Received | Jan 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070052
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.