510(k) K052210 ยท MQP Spinal Vertebral Body Replacement Device
NUVASIVE COROENT EXTENSURE SYSTEM
| Applicant | Nuvasive, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Dec 12, 2005 |
| Received | Aug 15, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052210
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.