510(k) K123578 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Weigao Orthopaedic Device Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Feb 1, 2013 |
| Received | Nov 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123578
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.