510(k) K873826 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION
| Applicant | Acromed Corp., Martinez CA, US |
| Decision | Substantially Equivalent, Nov 30, 1988 |
| Received | Sep 23, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873826
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.