FDA Product Code
FDA Product Code KWM — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.3800
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K880156 | VOLZ TOTAL WRIST PROSTHESIS | Biomet, Inc. | 1988-02-17 | Traditional | PDF ↗ |
| K872502 | M.W.P. WRIST PROSTHESIS | Protek, Inc. | 1987-07-23 | Traditional | PDF ↗ |
| K803031 | LAURE WRIST IMPLANT | Laure Prosthetics, Inc. | 1982-06-29 | Traditional | PDF ↗ |
| K800602 | TALEISNIK TOTAL WRIST PROSTHESIS | Dow Corning Wright | 1980-08-27 | Traditional | PDF ↗ |
| K801157 | WEBER-MAYO WRIST | Depuy, Inc. | 1980-08-04 | Traditional | PDF ↗ |
| K790774 | LODA WRIST PROSTHESIS | Depuy, Inc. | 1979-08-03 | Traditional | PDF ↗ |
Product code KWM · Class II · Orthopedic. Data: openFDA.