510(k) K121176 ยท MQP Spinal Vertebral Body Replacement Device
STGC
| Applicant | Cardinal Spine, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Aug 17, 2012 |
| Received | Apr 18, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121176
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.