Stryker Corporate · Class II · Cleared Oct 31, 2014
| K-number | K141941 |
| Device name | SPINEMASK TRACKER, SPINEMAP 3D 3.0-SOFTWARE,SPINEMAP 3D 3.0-UPGREADE, SPINEMAP 3D 3.0-ENABLE, SPINEMAP 3D 3.0-SALES D |
| Applicant | Stryker Corporate |
| Product code | OLO |
| Device class | Class II |
| Decision date | Oct 31, 2014 |
| Decision | Substantially Equivalent |
| Regulation | 882.4560 |
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