K-number	K202298
Device name	Lucent XP, Lucent XP Curved
Applicant	Spinal Elements, Inc.
Product code	MAX
Device class	Class II
Decision date	Dec 22, 2020
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Lucent XP, Lucent XP Curved

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