K-number	K131851
Device name	OSTEOMED NEURO RONGEUR
Applicant	Osteomed
Product code	HAE
Device class	Class II
Decision date	Dec 6, 2013
Decision	Substantially Equivalent
Regulation	882.4840

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View the full FDA submission: accessdata.fda.gov

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OSTEOMED NEURO RONGEUR

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