510(k) K030500 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ORIA ZENITH
| Applicant | Ortho Tec, LLC, California CA, US |
| Decision | Substantially Equivalent, Mar 20, 2003 |
| Received | Feb 19, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030500
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.