510(k) K161703 ยท HRS Plate, Fixation, Bone
LOQTEQ Distal Fibula Plate 3.5, Cancellous Screw 4.0, Washer
| Applicant | Aap Implantate AG, Berlin, DE |
| Decision | Substantially Equivalent, Nov 4, 2016 |
| Received | Jun 20, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161703
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.