KWM — Prosthesis, Wrist, Semi-Constrained Class II
FDA Device Classification
Classification Details
- Product Code
- KWM
- Device Class
- Class II
- Regulation Number
- 888.3800
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- Yes
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K880156 | biomet | VOLZ TOTAL WRIST PROSTHESIS | February 17, 1988 |
| K872502 | protek | M.W.P. WRIST PROSTHESIS | July 23, 1987 |
| K803031 | laure prosthetics | LAURE WRIST IMPLANT | June 29, 1982 |
| K800602 | dow corning wright | TALEISNIK TOTAL WRIST PROSTHESIS | August 27, 1980 |
| K801157 | depuy | WEBER-MAYO WRIST | August 4, 1980 |
| K790774 | depuy | LODA WRIST PROSTHESIS | August 3, 1979 |