Class Class II

ATTUNE™ Total Knee System; ATTUNE™ Revision Sleeve LPS™ Femoral Adaptors (K253197)

K253197 2025-11-19 Traditional
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Description

ATTUNE™ Total Knee System; ATTUNE™ Revision Sleeve LPS™ Femoral Adaptors by Depuy Ireland UC, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253197
Clearance Date2025-11-19
Clearance TypeTraditional
Product CodeJWH
Regulation Number888.3560

Categories

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