K-number	K150468
Device name	Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs
Applicant	K2 Medical GmbH & Co. KG
Product code	HAE
Device class	Class II
Decision date	Feb 29, 2016
Decision	Substantially Equivalent
Regulation	882.4840

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Source

View the full FDA submission: accessdata.fda.gov

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Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs

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