K-number	K980595
Device name	DEPUY ORTHOTECH CATERA SUTURE ANCHOR
Applicant	DePuy Orthopaedics, Inc.
Product code	MBI
Device class	Class II
Decision date	May 11, 1998
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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DEPUY ORTHOTECH CATERA SUTURE ANCHOR

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