510(k) K994308 ยท MRW System, Facet Screw Spinal Device
NUVASIVE TOWNLEY FACET SCREW
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Apr 18, 2000 |
| Received | Dec 21, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994308
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.