510(k) K113559 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS
| Applicant | Ldr Spine USA, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Dec 29, 2011 |
| Received | Dec 1, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113559
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.