K-number	K033506
Device name	COMPREHENSIVE HUMERAL FRACTURE POSITIONING SLEEVE
Applicant	Biomet, Inc.
Product code	KWS
Device class	Class II
Decision date	Feb 2, 2004
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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COMPREHENSIVE HUMERAL FRACTURE POSITIONING SLEEVE

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