K-number	K202768
Device name	KOSMO Femoral Stem
Applicant	B-One Ortho, Corp.
Product code	LZO
Device class	Class II
Decision date	Apr 1, 2021
Decision	Substantially Equivalent
Regulation	888.3353

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Source

View the full FDA submission: accessdata.fda.gov

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KOSMO Femoral Stem

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