K-number	K233264
Device name	Anthogyr INTEGRAL Guided Surgery Cassettes
Applicant	Anthogyr
Product code	KCT
Device class	Class II
Decision date	Dec 22, 2023
Decision	Substantially Equivalent
Regulation	880.6850

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Source

View the full FDA submission: accessdata.fda.gov

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Anthogyr INTEGRAL Guided Surgery Cassettes

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