510(k) K161129 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
PILLAR SA PTC
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, Sep 8, 2016 |
| Received | Apr 21, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161129
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.