Class Class II

Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates (K252807)

K252807 2026-01-12 Traditional
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Description

Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252807
Clearance Date2026-01-12
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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