K-number	K060177
Device name	KLS MARTIN RIGID FIXATION - STERILE
Applicant	KLS Martin L.P.
Product code	JEY
Device class	Class II
Decision date	Apr 18, 2006
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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KLS MARTIN RIGID FIXATION - STERILE

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