KMD — Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Composite Class II
FDA product code KMD covers "Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Composite", a Class II medical device regulated under 21 CFR 888.3100. Submissions are reviewed by the Orthopedic panel. Devices under this code are implants.
Classification Details
- Product Code
- KMD
- Device Class
- Class II
- Regulation Number
- 888.3100
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- Yes