510(k) K150449 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
LITe Plate System
| Applicant | Stryker Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Mar 20, 2015 |
| Received | Feb 20, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150449
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.