510(k) K091088 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
LDR SPINE CERVICAL INTERBODY FUSION SYSTEM
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Jul 14, 2009 |
| Received | Apr 15, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091088
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.