LGE
- Product code
- LGE
- Device name
- Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Trunnion-Bearing
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3530
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (all years, FDA)
- 2 (all years; only the last 3 years are listed here)
Official FDA classification page: LGE
Classification and pathway per current FDA publications. Data from openFDA (CC0).