K-number	K180213
Device name	Titanium TomoFix Medial High Tibia Plate Anatomical
Applicant	Synthes (USA) Products, LLC
Product code	HRS
Device class	Class II
Decision date	Oct 19, 2018
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Titanium TomoFix Medial High Tibia Plate Anatomical

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