510(k) K190261 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
BOSS Toe Fixation System
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Aug 14, 2019 |
| Received | Feb 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190261
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.