510(k) K100191 ยท KWP Appliance, Fixation, Spinal Interlaminal
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
| Applicant | Lanx, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Apr 15, 2010 |
| Received | Jan 22, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100191
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.