510(k) K033961 ยท KWP Appliance, Fixation, Spinal Interlaminal
ALTIUS OCT SYSTEM
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Apr 14, 2004 |
| Received | Dec 22, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033961
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.