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Appliance, Fixation, Spinal Interlaminal

FDA product code KWP · 408 cleared devices

Class 2 Orthopedic
Regulation
21 CFR 888.3050
Review panel
OR
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1978-09-27 – 2013-12-11
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