510(k) K920102 ยท KWP Appliance, Fixation, Spinal Interlaminal
THE SELBY SYSTEM
| Applicant | Advanced Spine Fixation Systems, Inc., Washington DC, US |
| Decision | Substantially Equivalent, May 5, 1992 |
| Received | Jan 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920102
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.