K-number	K212431
Device name	Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve
Applicant	Biomet, Inc.
Product code	JDG
Device class	Class II
Decision date	Feb 7, 2022
Decision	Substantially Equivalent
Regulation	888.3360

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Source

View the full FDA submission: accessdata.fda.gov

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Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve

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