K-number	K190446
Device name	Responsive Arthroscopy Wedge Push-In Suture Anchors
Applicant	Responsive Arthroscopy, LLC
Product code	MBI
Device class	Class II
Decision date	Mar 27, 2019
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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Responsive Arthroscopy Wedge Push-In Suture Anchors

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