Northern Orthopaedic Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K951028 | HAMEX TWO | December 11, 1995 |
| K951029 | HAMEX ONE | September 15, 1995 |