K-number	K864070
Device name	WHITESIDE ORTHOLOC (TM)
Applicant	Dow Corning Wright
Product code	HRY
Device class	Class II
Decision date	Jan 27, 1987
Decision	Substantially Equivalent for Some Indications
Regulation	888.3530

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View the full FDA submission: accessdata.fda.gov

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WHITESIDE ORTHOLOC (TM)

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