510(k) K010515 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO SYNERGY SPINAL SYSTEM
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 22, 2001 |
| Received | Feb 22, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K010515
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.