510(k) K023319 ยท MQP Spinal Vertebral Body Replacement Device
NUVASIVE MASH
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 4, 2003 |
| Received | Oct 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023319
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.