510(k) K043206 ยท MQP Spinal Vertebral Body Replacement Device
PIONEER VERTEBRAL BODY REPLACEMENT DEVICE (PIONEER VERTEBRAL SPACER)
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Jan 21, 2005 |
| Received | Nov 19, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043206
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.