510(k) K964007 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
ACROMED CABLE/WIRE PEDICLE SCREW
| Applicant | Acromed Corp., Cleveland OH, US |
| Decision | Substantially Equivalent for Some Indications, Dec 16, 1996 |
| Received | Oct 7, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964007
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.