510(k) K143228 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Ancora LLC Interbody Fusion Device
| Applicant | Frontier Medical Devices, Inc., Gwinn MI, US |
| Decision | Substantially Equivalent, Feb 26, 2015 |
| Received | Nov 10, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143228
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.