510(k) K110843 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ALEUTIAN SPACER SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Jun 22, 2011 |
| Received | Mar 25, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110843
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.