510(k) K895296 ยท KWP Appliance, Fixation, Spinal Interlaminal
SELBY II INSTRUMENTATION
| Applicant | Advanced Spine Fixation, Washington, D.C. DC, US |
| Decision | Substantially Equivalent for Some Indications, Mar 20, 1990 |
| Received | Aug 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895296
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.