510(k) K071922 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC
| Applicant | Rsb Spine, LLC, Chesterland OH, US |
| Decision | Substantially Equivalent, Sep 18, 2007 |
| Received | Jul 12, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071922
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.