K-number	K190483
Device name	SPIRA Open Matrix ALIF and LLIF
Applicant	Camber Spine Technologies
Product code	MAX
Device class	Class II
Decision date	Sep 23, 2019
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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SPIRA Open Matrix ALIF and LLIF

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