K-number	K221848
Device name	prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments
Applicant	Centinel Spine, LLC
Product code	QLQ
Device class	Class II
Decision date	Aug 19, 2022
Decision	Substantially Equivalent
Regulation	888.4515

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Source

View the full FDA submission: accessdata.fda.gov

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prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments

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