K-number	K241932
Device name	OSSIOfiber® Compression Staple
Applicant	OSSIO , Ltd.
Product code	MNU
Device class	Class II
Decision date	Aug 28, 2024
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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OSSIOfiber® Compression Staple

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