K-number	K202810
Device name	AutoStrut G2
Applicant	Orthospin, Ltd.
Product code	KTT
Device class	Class II
Decision date	Jan 6, 2021
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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AutoStrut G2

Everything you need for a 510(k) submission. Nothing you don't.