K-number	K233972
Device name	Camber Sacroiliac (SI) Fixation System
Applicant	Camber Spine Technologies
Product code	OUR
Device class	Class II
Decision date	Feb 27, 2024
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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