510(k) K970462 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
ACROMED ANTERIOR CERVICAL STABILIZATION SYSTEM
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent, Apr 3, 1997 |
| Received | Feb 6, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970462
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.