Cohort Medical Products Group, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K964975 | COHORT DISCECTOMY SYSTEMS (CDS) | February 24, 1997 |
| K950011 | COHORT(TM) ANTERIOR PLATE SYSTEM (APS) | November 6, 1995 |
| K943804 | BONE SCREW | December 8, 1994 |
| K943472 | COHORT AVB RETRACTOR SYSTEM | October 20, 1994 |
| K943474 | CANNULATED BONE SCREW | October 14, 1994 |