KWF — Prosthesis, Finger, Polymer Class II
FDA product code KWF covers "Prosthesis, Finger, Polymer", a Class II medical device regulated under 21 CFR 888.3230. Submissions are reviewed by the Orthopedic panel. Devices under this code are implants.
Classification Details
- Product Code
- KWF
- Device Class
- Class II
- Regulation Number
- 888.3230
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- Yes