K-number	K213420
Device name	WaveForm L System, WaveForm TO System, WaveForm TA System
Applicant	SeaSpine Orthopedics Corporation
Product code	MAX
Device class	Class II
Decision date	May 4, 2022
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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WaveForm L System, WaveForm TO System, WaveForm TA System

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