510(k) K131200 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ASPIRON ACP SYSTEM
| Applicant | U&I Corporation, Uijeongbu-Si, Gyeonggi-Do, KR |
| Decision | Substantially Equivalent, Aug 29, 2013 |
| Received | Apr 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131200
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.