510(k) K103169 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ALEUTTIAN
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Mar 7, 2011 |
| Received | Oct 27, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103169
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.