510(k) K111119 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
TRABECULAR METAL (TM) FUSION DEVICE
| Applicant | Zimmer Spine, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Nov 23, 2011 |
| Received | Apr 21, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111119
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.