K-number	K230851
Device name	Kodiak Lumbar Spacer System
Applicant	Met One Technologies, LLC
Product code	MAX
Device class	Class II
Decision date	May 26, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Kodiak Lumbar Spacer System

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