510(k) K161894 ยท HWC Screw, Fixation, Bone
SurgTech Trauma System
| Applicant | Surgtech, Inc., Westlake OH, US |
| Decision | Substantially Equivalent, Feb 21, 2017 |
| Received | Jul 11, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161894
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.