510(k) K950999 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS
| Applicant | Buckman Co., Inc., Concord CA, US |
| Decision | Substantially Equivalent, Jan 25, 1996 |
| Received | Mar 3, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950999
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.