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Prosthesis, Wrist, Hemi-, Ulnar

FDA product code KXE · 15 cleared devices

Class 2 Orthopedic
Regulation
21 CFR 888.3810
Review panel
OR
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1979-02-08 – 2019-05-03
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