K-number	K832301
Device name	DIRECT BONDED BRACKET REMOVER
Applicant	Northwest Orthopedics
Product code	JCX
Device class	Class II
Decision date	Aug 31, 1983
Decision	Substantially Equivalent
Regulation	878.4780

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View the full FDA submission: accessdata.fda.gov

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DIRECT BONDED BRACKET REMOVER

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