510(k) K043229 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION TO ALTIUS OCT SYSTEM
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Dec 21, 2004 |
| Received | Nov 22, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K043229
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.