K-number	K221324
Device name	ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)
Applicant	Camber Spine Technologies
Product code	OVD
Device class	Class II
Decision date	Mar 30, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)

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