510(k) K182055 · KWQ Appliance, Fixation, Spinal Intervertebral Body
SECULOK ACP System
| Applicant | U&I Corporation, Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Sep 10, 2018 |
| Received | Jul 31, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182055
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.