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DEPUY ATTUNE TOTAL KNEE SYSTEM

K103756 Class II Traditional
Decision Date
2011-03-15
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K103756
Product Code OIY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3560
Decision Date 2011-03-15
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 K103756, sponsored by DePuy Orthopaedics, 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 2011-03-15.

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.