510(k) K021679 ยท KWP Appliance, Fixation, Spinal Interlaminal
ORIA SPINAL CLIP SYSTEM
| Applicant | Ortho Tec, LLC, California CA, US |
| Decision | Substantially Equivalent, Nov 19, 2002 |
| Received | May 21, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021679
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.