510(k) K160791 ยท HWC Screw, Fixation, Bone
AmorChem Titanium Porous Fixation Device
| Applicant | Amorchem Holdings, Inc., Montreal, CA |
| Decision | Substantially Equivalent, Nov 15, 2016 |
| Received | Mar 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160791
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.