510(k) K062317 ยท MNH Orthosis, Spondylolisthesis Spinal Fixation
MODIFICATION TO NUVASIVE SPHERX II SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Sep 1, 2006 |
| Received | Aug 9, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062317
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.