510(k) K223069 · KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

Modular Rotating Hinge Knee Systems and Compatible Components

Applicant	Howmedica Osteonics Corp., Dba Stryker Orthopaedics, Mahwah NJ, US
Decision	Substantially Equivalent, Apr 21, 2023
Received	Sep 30, 2022
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K223069

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.