510(k) K051454 ยท MQP Spinal Vertebral Body Replacement Device
ALEUTIAN SPACER SYSTEM
| Applicant | K2m, LLC, Leesburg VA, US |
| Decision | Substantially Equivalent, Jul 27, 2005 |
| Received | Jun 2, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051454
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.