510(k) K914362 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS
| Applicant | Acorn Group, Inc., Walnut Creek CA, US |
| Decision | Substantially Equivalent, Apr 29, 1992 |
| Received | Oct 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914362
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.