Stryker Craniomaxillofacial
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232350 | Stryker Facial iD System | January 13, 2024 |
| K092743 | THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM | January 15, 2010 |
| K070876 | STRYKER TWIST DRILLS | April 27, 2007 |