K-number	K080678
Device name	UNI-KNEE 2.0
Applicant	Brainlab AG
Product code	HAW
Device class	Class II
Decision date	Jun 6, 2008
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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UNI-KNEE 2.0

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