KFX — Assembly, Thigh/Knee/Shank/Ankle/Foot, External Class II
FDA Device Classification
Classification Details
- Product Code
- KFX
- Device Class
- Class II
- Regulation Number
- 890.3500
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K932184 | vascutech | STERILE LEMAITRE GLOW 'N TELL TAPE | July 22, 1993 |
| K833868 | ipos luneburg | IPOS G.L.P. SYSTEM | November 28, 1983 |
| K830285 | besco financial service | REGNELL HYDRAULIC FEMORAL PROTHESIS | March 9, 1983 |
| K822240 | american mcgaw | ETHYLENE OXIDE STERILIZ. PARAMETRIC REL. | December 30, 1982 |