K-number	K002423
Device name	LACTOSORB PUSH SCREW
Applicant	Biomet, Inc.
Product code	DZL
Device class	Class II
Decision date	Oct 20, 2000
Decision	Substantially Equivalent
Regulation	872.4880

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View the full FDA submission: accessdata.fda.gov

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LACTOSORB PUSH SCREW

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