K-number	K233703
Device name	Bone Anchor (NGS-BA-01)
Applicant	ClearPoint Neuro, Inc.
Product code	HAW
Device class	Class II
Decision date	Apr 26, 2024
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Bone Anchor (NGS-BA-01)

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