510(k) K102401 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
HEMI IMPLANT; MINI HEMI IMPLANT
| Applicant | Vilex, Inc., Mcminnville TN, US |
| Decision | Substantially Equivalent, Jul 20, 2011 |
| Received | Aug 24, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102401
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.