510(k) K051525 ยท MQP Spinal Vertebral Body Replacement Device
ARX SPINAL SYSTEM
| Applicant | Amedica Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 17, 2006 |
| Received | Jun 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051525
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.