510(k) K131512 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
KATIA SYSTEM
| Applicant | Shanghai Sanyou Medical Co, Ltd., Bartlett TN, US |
| Decision | Substantially Equivalent, Aug 7, 2013 |
| Received | May 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131512
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.