FDA 510(k), K093677, STRYKER ARTHROSCOPE

FDA 510(k), K093677, STRYKER ARTHROSCOPE

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510(K) Number: K093677
Device Name: STRYKER ARTHROSCOPE
Manufacturer:
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 11/27/2009
Decision Date: 03/05/2010
Regulation Medical Specialty: Orthopedic
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