K-number	K082215
Device name	OSTEORAPTOR SUTURE ANCHOR
Applicant	Smith & Nephew Inc., Endoscopy Division
Product code	JDR
Device class	Class II
Decision date	Nov 3, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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OSTEORAPTOR SUTURE ANCHOR

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