510(k) K121808 ยท KWP Appliance, Fixation, Spinal Interlaminal
CASIAN, 3.5/4.5 CONNECTORS
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Jul 20, 2012 |
| Received | Jun 20, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121808
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.