510(k) K190543 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
Cannulated Hemi Implant
| Applicant | Vilex IN Tennessee, Inc., Mcminnville TN, US |
| Decision | Substantially Equivalent, May 31, 2019 |
| Received | Mar 4, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190543
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.