510(k) K223528

Device
Triathlon® Hinge Knee System
Applicant
Howmedica Osteonics Corp., Dba Stryker Orthopaedics
510(k) number
K223528
Product code
KRO
Decision
Substantially Equivalent (SESE)
Decision date
2023-01-20
Date received
2022-11-23
Regulation
888.3510
Classification name
Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Allison Byrne
Address
325 Corporate Dr. Mahwah NJ US 07430 07430

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code KRO

510(k)DeviceApplicantDecision date
K252898Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella; Triathlon® Symmetric Patella; Triathlon® Asymmetric Patella; Scorpio® Universal Dome Patella; Triathlon® Hinge BumperHowmedica Osteonics Corp., Dba Stryker Orthopaedics2025-12-15
K252303Stem Extension Line (USTAR II System)United Orthopedic Corporation2025-08-22
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K210010GMK Revision & Hinge Extension - TiNbN CoatingMedacta International S.A.2021-03-02
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