510(k) K152454 ยท KWD Prosthesis, Toe, Hemi-, Phalangeal
HemiCAP MTP Resurfacing Hemi-Arthroplasty System
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Apr 11, 2016 |
| Received | Aug 28, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152454
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.