FDA.reportPublic FDA data

510(k) K242665

Device
DePuy ATTUNE? Total Knee System
Applicant
Depuy Orthopedics, Inc.
510(k) number
K242665
Product code
OIY
Decision
Substantially Equivalent (SESE)
Decision date
2024-11-01
Date received
2024-09-04
Regulation
888.3560
Classification name
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Christina Kaucic
Address
700 Orthopaedic Dr. Warsaw IN US 46582 46582

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code OIY#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252887DePuy ATTUNE™ Knee SystemDePuy Orthopaedics, Inc.2026-05-22
K201347DePuy ATTUNE™ Total Knee SystemDePuy Orthopaedics, Inc.2020-06-18
K120038A200 KNEE SYSTEMRenovis Surgical Technologies, LLC2013-02-14
K121727MOVATION KNEE SYSTEMEncore Medical L.P.2012-08-15
K113756HIGHLY CROSS LINKED VE CENTRAL PEG PATELLA HIGHLY CROSS LINKED VE TRI-PEG PATELLA HIGHLY CROSS LINKED VE METAL BACKED PAEncore Medical L.P.2012-03-14
K111433DEPUY STTUNE (TM) PS KNEE SYSTEMDePuy Orthopaedics, Inc.2011-08-30
K103756DEPUY ATTUNE TOTAL KNEE SYSTEMDePuy Orthopaedics, Inc.2011-03-15
K103223HIGHLY CROSS-LINKED VITAMIN E UHMWPE TIBIAL INSERTSEncore Medical L.P.2010-12-21
K101433DEPUY ATTUNE KNEE SYSTEMDePuy Orthopaedics, Inc.2010-12-10
K091956HIGHLY CROSS-LINKED VITAMIN E UHMWPE TIBIAL INSERTS, MODEL 391/392-09_19-702_712Encore Medical L.P.2010-09-28
K100048E1 ANTIOXIDANT INFUSED TECHNOLOGYBiomet Manufacturing Corp2010-03-09