Global Orthopaedic Technology, USA, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K050473 | RBK PATELLA FEMORAL KNEE | November 14, 2005 |
| K051721 | GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM | October 26, 2005 |
| K033351 | GLOBAL RESURFACING UNICOMPARTMENTAL (GRU) KNEE | March 11, 2004 |