KWO — Prosthesis, Wrist, Carpal Scaphoid Class II
FDA product code KWO covers "Prosthesis, Wrist, Carpal Scaphoid", a Class II medical device regulated under 21 CFR 888.3760. Submissions are reviewed by the Orthopedic panel. Devices under this code are implants. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KWO
- Device Class
- Class II
- Regulation Number
- 888.3760
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K864490 | dow corning wright | SWANSON TITANIUM CARPAL SCAPHOID IMPLANT | April 15, 1987 |