510(k) K080526 ยท KWP Appliance, Fixation, Spinal Interlaminal
SIERRA SYSTEM
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Apr 16, 2008 |
| Received | Feb 26, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080526
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.