510(k) K042034 ยท FST Light, Surgical, Fiberoptic
NUVASIVE MAXCESS LIGHT GUIDE
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Oct 26, 2004 |
| Received | Jul 29, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042034
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.