Class Class II

Syndesmosis TightRope PRO (K253727)

K253727 2025-12-22 Special
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Description

Syndesmosis TightRope PRO by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253727
Clearance Date2025-12-22
Clearance TypeSpecial
Product CodeHTN
Regulation Number888.3030

Categories

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