Prosthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/composite

Device Code: 4588

Product Code(s): KYK

Device Classification Information

Device Type ID4588
Device NameProsthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/composite
Regulation DescriptionKnee Joint Femorotibial Metal/composite Semi-constrained Cemented Prosthesis.
Regulation Medical SpecialtyOrthopedic
Review PanelOrthopedic
Premarket Review Office Of Device Evaluation (ODE)
Division Of Orthopedic Devices (DOD)
Joint And Fixation Devices Branch One ¿ Knees/Shoulders/Elbows/Ankles/Toes (JFDB1)
Submission Type510(k)
CFR Regulation Number888.3500 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeKYK
GMP ExemptNo
Summary MREligible
Implanted DeviceYes
Life Support DeviceNo
Third Party Review Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

Device Type ID4588
DeviceProsthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/composite
Product CodeKYK
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionKnee Joint Femorotibial Metal/composite Semi-constrained Cemented Prosthesis.
CFR Regulation Number888.3500 [🔎]
TPLC Last Update: 2019-04-02 20:52:19

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