510(k) K023684 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365
| Applicant | Vilex, Inc., Pleasant Hills PA, US |
| Decision | Substantially Equivalent, Mar 1, 2004 |
| Received | Nov 1, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023684
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.