510(k) K090343 ยท KWP Appliance, Fixation, Spinal Interlaminal
SENTINEL SPINAL SYSTEM
| Applicant | Life Spine, Hoffman Estates IL, US |
| Decision | Substantially Equivalent, Aug 11, 2009 |
| Received | Feb 10, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090343
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.