K-number	K241609
Device name	Tornier Humeral Reconstruction System (Tornier HRS)
Applicant	Stryker Corporation (Tornier, Inc.)
Product code	KWS
Device class	Class II
Decision date	Sep 10, 2024
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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Tornier Humeral Reconstruction System (Tornier HRS)

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