510(k) K172213 ยท HWC Screw, Fixation, Bone
MECRON Cannulated Screw System
| Applicant | Merete GmbH, Berlin, DE |
| Decision | Substantially Equivalent, Oct 23, 2017 |
| Received | Jul 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172213
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.