510(k) K121979 ยท KWP Appliance, Fixation, Spinal Interlaminal
PASS OCT SPINAL SYSTEM
| Applicant | Medicrea International, Neyron, FR |
| Decision | Substantially Equivalent, Mar 21, 2013 |
| Received | Jul 6, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121979
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.