K-number	K050028
Device name	MAESTRO CARPAL HEMIARTHROPLASTY
Applicant	Biomet Manufacturing, Inc.
Product code	KWN
Device class	Class II
Decision date	Mar 25, 2005
Decision	Substantially Equivalent
Regulation	888.3750

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View the full FDA submission: accessdata.fda.gov

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MAESTRO CARPAL HEMIARTHROPLASTY

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