K-number	K231769
Device name	activL® Next Generation Instrumentation
Applicant	Aesculap Implants Systems, LLC
Product code	QLQ
Device class	Class II
Decision date	Jul 13, 2023
Decision	Substantially Equivalent
Regulation	888.4515

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Source

View the full FDA submission: accessdata.fda.gov

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activL® Next Generation Instrumentation

Everything you need for a 510(k) submission. Nothing you don't.