510(k) K110327 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
LDR SPINE ROI-A INTERBODY FUSION SYSTEM
| Applicant | Ldr Spine USA, Austin TX, US |
| Decision | Substantially Equivalent, Sep 30, 2011 |
| Received | Feb 3, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110327
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.