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Appliance, Facial Fracture, External

FDA product code FYI · 4 cleared devices

Class 1 General, Plastic Surgery
Regulation
21 CFR 878.3250
Review panel
SU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1979-11-05 – 1987-05-11
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