K-number	K213199
Device name	Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System
Applicant	Stryker GmbH
Product code	HWC
Device class	Class II
Decision date	Jan 11, 2022
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System

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