FDA 510(k), K133281, NEOTRACT UROLIFT SYSTEM

FDA 510(k), K133281, NEOTRACT UROLIFT SYSTEM

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510(K) Number: K133281
Device Name: NEOTRACT UROLIFT SYSTEM
Manufacturer:
Device Classification Name: Implantable Transprostatic Tissue Retractor System
Regulation Number: 876.5530
Classification Product Code: PEW
Date Received: 10/25/2013
Decision Date: 12/20/2013
Regulation Medical Specialty: Gastroenterology/Urology
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