K-number	K243137
Device name	Curiteva Porous PEEK Laminoplasty System
Applicant	Curiteva, Inc.
Product code	NQW
Device class	Class II
Decision date	Oct 28, 2024
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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Curiteva Porous PEEK Laminoplasty System

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