K-number	K955640
Device name	LORENZ MANDIBULAR DISTRACTOR
Applicant	Biomet, Inc.
Product code	MQN
Device class	Class II
Decision date	Feb 14, 1996
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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LORENZ MANDIBULAR DISTRACTOR

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