K-number	K950595
Device name	LUHR MANDIBULAR/SMALL FIXATION IMPLANTS
Applicant	Howmedica Corp.
Product code	JEY
Device class	Class II
Decision date	Jul 12, 1995
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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LUHR MANDIBULAR/SMALL FIXATION IMPLANTS

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