Class Class II

Tornier Humeral Reconstruction System (Tornier HRS) (K241609)

K241609 2024-09-10 Traditional
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Description

Tornier Humeral Reconstruction System (Tornier HRS) by Stryker Corporation (Tornier, Inc.) — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241609
Clearance Date2024-09-10
Clearance TypeTraditional
Product CodeKWS
Regulation Number888.3660

Categories

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