LGE
1999-08-12
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Trunnion-Bearing
FDA product code LGE · 2 cleared devices
Class 2
Orthopedic
- Regulation
- 21 CFR 888.3530
- Review panel
- OR
- Implant
- Yes
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1981-07-01 – 1999-08-12
LGE
1981-07-01
KINEMATIC ROTATING HINGE TOTAL KNEE PR.
View details →No matching devices.
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