K-number	K012872
Device name	RESORBABLE SCREW ANCHOR
Applicant	Arthrotek, Inc.
Product code	HWC
Device class	Class II
Decision date	Nov 20, 2001
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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RESORBABLE SCREW ANCHOR

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