510(k) K884161 ยท KWP Appliance, Fixation, Spinal Interlaminal
ACROMED ILIAC SCREW
| Applicant | Buckman Co., Inc., Martinez CA, US |
| Decision | Substantially Equivalent for Some Indications, May 3, 1989 |
| Received | Oct 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884161
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.