510(k) K081883 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM
| Applicant | Us Spine, Apple Valley MN, US |
| Decision | Substantially Equivalent, Sep 24, 2008 |
| Received | Jul 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081883
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.