FDA 510(k), K140903, NUVIS ARTHROSCOPE

FDA 510(k), K140903, NUVIS ARTHROSCOPE

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510(K) Number: K140903
Device Name: NUVIS ARTHROSCOPE
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/09/2014
Decision Date: 07/17/2014
Regulation Medical Specialty: Orthopedic
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