K-number	K980760
Device name	KLS-MARTIN MMF SCREW
Applicant	KLS-Martin L.P.
Product code	DZL
Device class	Class II
Decision date	Dec 21, 1999
Decision	Substantially Equivalent
Regulation	872.4880

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View the full FDA submission: accessdata.fda.gov

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KLS-MARTIN MMF SCREW

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