K-number	K223631
Device name	Comprehensive Segmental Revision System(SRS)
Applicant	Biomet Orthopedics
Product code	KWT
Device class	Class II
Decision date	Jul 12, 2023
Decision	Substantially Equivalent
Regulation	888.3650

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Source

View the full FDA submission: accessdata.fda.gov

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Comprehensive Segmental Revision System(SRS)

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