Stryker Corporation · Class II · Cleared Jan 20, 2016
| K-number | K151726 |
| Device name | AVS AL and AVS ALign PEEK Spacers, AVS PL and AVS UniLIF PEEK Spacers, AVS TL PEEK Spacer, AVS Navigator PEEK Spacer, AVS ARIA PEEK Spacer |
| Applicant | Stryker Corporation |
| Product code | MAX |
| Device class | Class II |
| Decision date | Jan 20, 2016 |
| 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