510(k) K894472 ยท KWP Appliance, Fixation, Spinal Interlaminal
CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL
| Applicant | Buckman Co., Inc., Martinez CA, US |
| Decision | Substantially Equivalent, Oct 10, 1989 |
| Received | Jul 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894472
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.