510(k) K113601 ยท HRS Plate, Fixation, Bone
AAP LOQTEQ DISTAL MEDIAL TIBIA PLATE 3.5 SYSTEM
| Applicant | Aap Implantate AG, Berlin, DE |
| Decision | Substantially Equivalent, Nov 8, 2012 |
| Received | Dec 5, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113601
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.