K-number	K182109
Device name	REDAPT Modular Acetabular Shell
Applicant	Smith & Nephew, Inc.
Product code	LPH
Device class	Class II
Decision date	Nov 16, 2018
Decision	Substantially Equivalent
Regulation	888.3358

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Source

View the full FDA submission: accessdata.fda.gov

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REDAPT Modular Acetabular Shell

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