510(k) K063399 ยท MQP Spinal Vertebral Body Replacement Device
ALEUTIAN SPACER SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Feb 23, 2007 |
| Received | Nov 9, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063399
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.