510(k) K923703 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
KANEDA ANTERIOR SPINAL MULTISEGMENTAL FIXATION DEV
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent for Some Indications, May 20, 1993 |
| Received | Jul 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923703
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.