510(k) K023884 ยท KWP Appliance, Fixation, Spinal Interlaminal
MODIFICATION ORIA SPINAL SYSTEM
| Applicant | Ortho Tec, LLC, California CA, US |
| Decision | Substantially Equivalent, Aug 20, 2003 |
| Received | Nov 21, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023884
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.