510(k) K895413 ยท KWP Appliance, Fixation, Spinal Interlaminal
ACROMED DOUBLE SUBLAMINAR WIRE
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent, Nov 22, 1989 |
| Received | Sep 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895413
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.