510(k) K161173 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Avenue® T TLIF Cage
| Applicant | Ldr Spine USA, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Sep 28, 2016 |
| Received | Apr 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161173
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.