KII — Tube, Cement Ventilation Class I
FDA product code KII covers "Tube, Cement Ventilation", a Class I medical device regulated under 21 CFR 888.4230. Submissions are reviewed by the Orthopedic panel.
Classification Details
- Product Code
- KII
- Device Class
- Class I
- Regulation Number
- 888.4230
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- No