510(k) K162380 ยท HRS Plate, Fixation, Bone
Locking Plate System
| Applicant | Beijing Keyi Medical Device Technology Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, May 2, 2017 |
| Received | Aug 24, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162380
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.