510(k) K070181 ยท MQP Spinal Vertebral Body Replacement Device
SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XX
| Applicant | Sintea Biotech, Inc., Miami Beach FL, US |
| Decision | Substantially Equivalent, Apr 18, 2007 |
| Received | Jan 19, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070181
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.