510(k) K090981 ยท NKB Thoracolumbosacral Pedicle Screw System
MODIFICATION TO: NUVASIVE SPHERX SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 2, 2009 |
| Received | Apr 7, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090981
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.