Stryker Instruments · Class II · Cleared Jun 25, 2021
| K-number | K211238 |
| Device name | SpineJack Expansion Kit, Vertaplex Radiopaque Bone Cement, Vertaplex HV Radiopaque Bone Cement |
| Applicant | Stryker Instruments |
| Product code | NDN |
| Device class | Class II |
| Decision date | Jun 25, 2021 |
| Decision | Substantially Equivalent |
| Regulation | 888.3027 |
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