510(k) K854524 ยท KWP Appliance, Fixation, Spinal Interlaminal
KIRSCHNER SPINAL PRODUCT SYSTEM
| Applicant | Kirschner Medical Corp., Timonium MD, US |
| Decision | Substantially Equivalent, Dec 9, 1985 |
| Received | Nov 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854524
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.