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Assembly, Thigh/Knee/Shank/Ankle/Foot, External

FDA product code KFX · 4 cleared devices

Class 2 Physical Medicine
Regulation
21 CFR 890.3500
Review panel
PM
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1982-12-30 – 1993-07-22
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