K-number	K222820
Device name	BRM TOOL Screws, BIOPLAN Subtalar Implant
Applicant	Brm Extremities
Product code	HWC
Device class	Class II
Decision date	Dec 16, 2022
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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BRM TOOL Screws, BIOPLAN Subtalar Implant

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