510(k) K131377 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
HEMICAP MTP RESURFACING HEMI-ARTHROPLASTY IMPLANT
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Nov 19, 2013 |
| Received | May 14, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131377
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.