Depuy Spine, A Johnson & Johnson Company
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K131802 | EXPEDIUM, VIPER. VIPER 2 SPINE SYSTEM | September 12, 2013 |
| K102249 | EXPEDIUM SPINE SYSTEM | December 16, 2010 |
| K071927 | MODIFICATION TO VERTEBROPLASTIC RADIOPAQUE BONE CEMENT | November 21, 2007 |
| K071495 | EXPEDIUM 4.5MM SPINE SYSTEM | June 29, 2007 |