K-number	K232471
Device name	Vy Spine VyLam Laminoplasty System
Applicant	Vy Spine, LLC
Product code	NQW
Device class	Class II
Decision date	Oct 10, 2023
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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Vy Spine VyLam Laminoplasty System

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Vy Spine VyLam Laminoplasty System