510(k) K163061 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
Altus Spine Cervical Plate System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Feb 6, 2017 |
| Received | Nov 1, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163061
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.