510(k) K143163 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK Spacer, AVS® Navigator PEEK Spacer, AVS® ARIA PEEK Spacer, AccuLIF TL and PL Cage, AVS® Anchor-L Spacer, Aero-AL Lumbar Cage System
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, Jan 26, 2015 |
| Received | Nov 3, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143163
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.