510(k) K903376 ยท KWP Appliance, Fixation, Spinal Interlaminal
ACROMED SACRAL SCREW
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent for Some Indications, Dec 27, 1990 |
| Received | Jul 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903376
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.