FDA 510(k) Applications for Medical Device Product Code: LGE (Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Trunnion-Bearing)

FDA 510(k) Applications for Medical Device Product Code "LGE"
(Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Trunnion-Bearing)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K992346	HOWMEDICA OSTEONICS CORP.	KINEMATIC II ROTATING HINGE KNEE	08/12/1999