510(k) K131782 ยท HRS Plate, Fixation, Bone
LOQTEQ HIGH TIBIA OSTEOTOMY PLATE 4.5
| Applicant | Aap Implantate AG, Berlin, DE |
| Decision | Substantially Equivalent, Nov 18, 2013 |
| Received | Jun 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131782
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.