K-number	K050752
Device name	AESCULAP ORTHOPILOT 2 THA V 2.0
Applicant	Aesculap, Inc.
Product code	HAW
Device class	Class II
Decision date	Apr 27, 2005
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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AESCULAP ORTHOPILOT 2 THA V 2.0

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