510(k) K101886 ยท MQP Spinal Vertebral Body Replacement Device
DSC/ALF SPINAL SYSTEM
| Applicant | Sintea Plastek, LLC, Miami Beach FL, US |
| Decision | Substantially Equivalent, Jul 21, 2011 |
| Received | Jul 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101886
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.