510(k) K113285 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
LDR SPINE USA AVENUE L INTERBODY FUSION
| Applicant | Ldr Spine USA, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Jul 26, 2012 |
| Received | Nov 7, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113285
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.