K-number	K960297
Device name	MANDIBULAR BONE DISTRACTOR II
Applicant	Howmedica Corp.
Product code	MQN
Device class	Class II
Decision date	Aug 6, 1996
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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MANDIBULAR BONE DISTRACTOR II

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