Stryker Corporation · Class II · Cleared Jan 26, 2015
| K-number | K143163 |
| Device name | 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 |
| Product code | OVD |
| Device class | Class II |
| Decision date | Jan 26, 2015 |
| Decision | Substantially Equivalent |
| Regulation | 888.3080 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov