K-number	K203503
Device name	Camber Sacroiliac (SI) Fixation System
Applicant	Camber Spine Technologies, LLC
Product code	OUR
Device class	Class II
Decision date	Sep 2, 2022
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Camber Sacroiliac (SI) Fixation System

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