K-number	K151615
Device name	TiTHON Staple with OsseoTi Technology
Applicant	Biomet Manufacturing Corp
Product code	JDR
Device class	Class II
Decision date	Oct 2, 2015
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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TiTHON Staple with OsseoTi Technology

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