510(k) K974757 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent for Some Indications, Mar 5, 1998 |
| Received | Dec 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974757
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.