510(k) K130859 ยท HWC Screw, Fixation, Bone
HAMMERTOE CORRECTION SYSTEM
| Applicant | Arthrosurface, Inc., Franklin MA, US |
| Decision | Substantially Equivalent, Jul 25, 2013 |
| Received | Mar 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130859
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.