Class Class II

Hoffmann LRF System (K253202)

K253202 2025-12-19 Traditional
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Description

Hoffmann LRF System by Stryker GmbH, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253202
Clearance Date2025-12-19
Clearance TypeTraditional
Product CodeKTT
Regulation Number888.3030

Categories

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