510(k) K070218 ยท MQP Spinal Vertebral Body Replacement Device
VERTIFLEX OCTANE PEEK VERTEBRAL BODY REPLACEMENT (PEEK VBR)
| Applicant | Vertiflex (Tm), Incorporated, Carlsbad CA, US |
| Decision | Substantially Equivalent, Apr 6, 2007 |
| Received | Jan 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070218
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.