510(k) K131724 ยท MQP Spinal Vertebral Body Replacement Device
PIONEER MAXFUSE VERTEBRAL BODY REPLACEMENT DEVICE
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Dec 24, 2013 |
| Received | Jun 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131724
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.