510(k) K142490 ยท HWC Screw, Fixation, Bone
ProxiFuse Hammer Toe Device
| Applicant | Cartiva, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Dec 15, 2014 |
| Received | Sep 4, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142490
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.