FDA 510(k), K151476, Beactive Brace

FDA 510(k), K151476, Beactive Brace

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510(K) Number: K151476
Device Name: Beactive Brace
Manufacturer: NATURES PILLOWS, INC.
Device Classification Name: orthosis, limb, for back pain
Regulation Number: 890.3475
Classification Product Code: PMV
Date Received: 06/02/2015
Decision Date: 02/26/2016
Regulation Medical Specialty: Physical Medicine

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