510(k) K020411 ยท MRW System, Facet Screw Spinal Device
NUVASIVE TRIAD FACET SCREW SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 12, 2002 |
| Received | Feb 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020411
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.