510(k) K080024 ยท MQP Spinal Vertebral Body Replacement Device
ALEUTIAN SPACER, MODEL K2-07-1004-01, K2-07-1005-01
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Jan 24, 2008 |
| Received | Jan 4, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080024
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.