510(k) K032476 ยท MQP Spinal Vertebral Body Replacement Device
NUVASIVE MESH
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Nov 13, 2003 |
| Received | Aug 12, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032476
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.