K-number	K190915
Device name	OsteoFab Suture Anchors
Applicant	Oxford Performance Materials, Inc.
Product code	MBI
Device class	Class II
Decision date	Jul 3, 2019
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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OsteoFab Suture Anchors

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