510(k) K161747 · HRS Plate, Fixation, Bone
LOQTEQ® VA Distal Tibia Plate System: LOQTEQ® VA Distal Medial Tibia Plate 3.5; LOQTEQ® VA Distal Anterolateral Tibia Plate 3.5; LOQTEQ® VA Distal Fibula Plate 2.7/3.5
| Applicant | Aap Implantate AG, Berlin, DE |
| Decision | Substantially Equivalent, Nov 22, 2016 |
| Received | Jun 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161747
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.