510(k) K161058 ยท HWC Screw, Fixation, Bone
Cannulated Screw
| Applicant | Miami Device Solutions, LLC, Miami FL, US |
| Decision | Substantially Equivalent, Jul 29, 2016 |
| Received | Apr 15, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161058
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.