K-number	K203385
Device name	TenoTac Soft Tissue Fixation System
Applicant	Paragon 28, Inc.
Product code	MBI
Device class	Class II
Decision date	Feb 11, 2021
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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TenoTac Soft Tissue Fixation System

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