Class Class II

Materialise TKA Guide System (K253793)

K253793 2026-01-06 Special
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Description

Materialise TKA Guide System by Materialise N.V, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253793
Clearance Date2026-01-06
Clearance TypeSpecial
Product CodeJWH
Regulation Number888.3560

Categories

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