K-number	K001793
Device name	SYNTHES SCALLOPED DISTAL TIBIA PLATE
Applicant	Synthes (Usa)
Product code	LXT
Device class	Class II
Decision date	Aug 17, 2000
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SYNTHES SCALLOPED DISTAL TIBIA PLATE

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