K-number	K192449
Device name	Joline Kyphoplasty System Allevo
Applicant	Joline GmbH & Co. KG
Product code	NDN
Device class	Class II
Decision date	May 27, 2020
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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Joline Kyphoplasty System Allevo

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