FDA 510(k), K083552, MAXMORESPINE TOM STICK

FDA 510(k), K083552, MAXMORESPINE TOM STICK

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510(K) Number: K083552
Device Name: MAXMORESPINE TOM STICK
Manufacturer: HOOGLAND SPINE PRODUCTS GMBH
Device Classification Name: arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 12/01/2008
Decision Date: 10/09/2009
Regulation Medical Specialty: Orthopedic

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