KRR
- Product code
- KRR
- Device name
- Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3540
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (all years, FDA)
- 27 (all years; only the last 3 years are listed here)
Official FDA classification page: KRR
Classification and pathway per current FDA publications. Data from openFDA (CC0).