510(k) K083562 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
STRYKER SPINE NULOCK ANTERIOR CERVICAL PLATING SYSTEM
| Applicant | Stryker Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Mar 25, 2009 |
| Received | Dec 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083562
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.