KWE
- Product code
- KWE
- Device name
- Prosthesis, Finger, Constrained, Metal, Uncemented
- Device class
- Class 3
- 21 CFR
- 21 CFR 888.3200
- Medical specialty
- Orthopedic
- Marketing pathway
- PMA
- Flag
- Implant
FDA classification definition
call for pmas to be filed by 12/26/96 per 61 FR 50709 on 9/27/96
Official FDA classification page: KWE
Classification and pathway per current FDA publications. Data from openFDA (CC0).