K-number	K061801
Device name	2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS
Applicant	Arthrotek, Inc.
Product code	JDR
Device class	Class II
Decision date	Aug 7, 2006
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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2.8 & 3.5MM LACTOSCREW SUTURE ANCHORS

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