K-number	K233893
Device name	AlphaVent Knotless SP PEEK Anchor
Applicant	Stryker Endoscopy
Product code	MBI
Device class	Class II
Decision date	Jan 25, 2024
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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AlphaVent Knotless SP PEEK Anchor

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