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DePuy ATTUNE™ Total Knee System

K242665 Class II Traditional
Decision Date
2024-11-01
Sponsor / Applicant
Depuy Orthopedics, Inc.

Technical Specification

510(k) Submission ID K242665
Product Code OIY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2024-11-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DePuy ATTUNE™ Total Knee System received FDA 510(k) clearance under submission number K242665, sponsored by Depuy Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2024-11-01.

Classification & Regulation

This clearance is catalogued under FDA product code OIY and 21 CFR 888.3560, within the Orthopedic review panel as a Class II device.