510(k) K121791 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ZOU ANTERIOR LUMBAR PLATE SYSTEM
| Applicant | Corelink, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Nov 19, 2012 |
| Received | Jun 19, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121791
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.