510(k) K884998 ยท KWP Appliance, Fixation, Spinal Interlaminal
SELBY INSTRUMENTATION
| Applicant | Advanced Spine Fixation Systems, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent for Some Indications, Jun 22, 1989 |
| Received | Dec 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884998
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.