K-number	K234092
Device name	SafeOp 3: Neural Informatix Systeem
Applicant	Alphatec Spine, Inc.
Product code	GWF
Device class	Class II
Decision date	Apr 19, 2024
Decision	Substantially Equivalent
Regulation	882.1870

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Source

View the full FDA submission: accessdata.fda.gov

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SafeOp 3: Neural Informatix Systeem

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