510(k) K092656 ยท KWP Appliance, Fixation, Spinal Interlaminal
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM
| Applicant | Lanx, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Nov 24, 2009 |
| Received | Aug 28, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092656
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.