510(k) K002592 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 6, 2000 |
| Received | Aug 21, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002592
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.