K-number	K160523
Device name	BrightMatter Guide with BrightMatter Pointer
Applicant	Synaptive Medical, Inc.
Product code	HAW
Device class	Class II
Decision date	Jun 24, 2016
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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BrightMatter Guide with BrightMatter Pointer

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