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Prosthesis, Ptfe/Carbon-Fiber

FDA product code KDA · 1 cleared devices

Class 2 General, Plastic Surgery
Regulation
21 CFR 878.3500
Review panel
SU
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1986-05-23 – 1986-05-23
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