K-number	K201219
Device name	Biocore9 Femoral Head Resurfacing Component
Applicant	Biocore9, LLC
Product code	KXA
Device class	Class II
Decision date	Jan 19, 2021
Decision	Substantially Equivalent
Regulation	888.3400

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Source

View the full FDA submission: accessdata.fda.gov

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Biocore9 Femoral Head Resurfacing Component

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