510(k) K982443 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
DOC VENTRAL CERVICAL STABILIZATION SYSTEM
| Applicant | Depuy Motech Acromed, Cleveland OH, US |
| Decision | Substantially Equivalent, Jul 29, 1998 |
| Received | Jul 14, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K982443
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.