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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

ATTUNE Revision Knee System

FDA 510(k) source

510(k) number
K262130
Applicant
Depuy Orthopaedics, Inc.
Decision date
Sep 4, 2026
Date received
Jun 24, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
JWH
Device type
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class
Class II
Regulation
21 CFR 888.3560
Advisory committee
Orthopedic
Statement or summary
Summary
Third party
N
Location
Warsaw, IN, US