510(k) K924474 ยท KWP Appliance, Fixation, Spinal Interlaminal
SELBY INSTRUMENTATION
| Applicant | Advanced Spine Fixation Systems, Inc., Stanton CA, US |
| Decision | Substantially Equivalent, Sep 21, 1993 |
| Received | Sep 3, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924474
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.