510(k) K101302 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ALEUTIAN IBF SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Jul 22, 2010 |
| Received | May 10, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101302
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.