Stryker Spine · Class II · Cleared Oct 7, 2008
| K-number | K082608 |
| Device name | RADIUS SPINAL SYSTEM, VITALLIUM ROD #486613601 |
| Applicant | Stryker Spine |
| Product code | NKB |
| Device class | Class II |
| Decision date | Oct 7, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 888.3070 |
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