K-number	K051721
Device name	GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM
Applicant	Global Orthopaedic Technology, USA, Inc.
Product code	HRY
Device class	Class II
Decision date	Oct 26, 2005
Decision	Substantially Equivalent
Regulation	888.3530

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View the full FDA submission: accessdata.fda.gov

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GLOBAL RESURFACING UNICOMPARTMENTAL KNEE SYSTEM

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